at they had no warning signs (sleep attack) such as excessive drowsiness, and believed that they were alert immediately prior to the event. some of these events had been reported as late as one year after the initiation of treatment. somnolence is a common occurrence in patients receiving pramipexole at doses above 1.5 mg/day (0.5 mg three times a day) for parkinson's disease. in controlled clinical trials in rls, patients treated with pramipexole dihydrochloride tablets at doses of 0.25 to 0.75 mg once a day, the incidence of somnolence was 6% compared to an incidence of 3% for placebo-treated patients [see adverse reactions (6.1) ]. it has been reported that falling asleep while engaged in activities of daily living usually occurs in a setting of preexisting somnolence, although patients may not give such a history. for this reason, prescribers should reassess patients for drowsiness or sleepiness, especially since some of the events occur well after the start of treatment. prescribers should also be aware that patients may not acknowledge drowsiness or sleepiness until directly questioned about drowsiness or sleepiness during specific activities. before initiating treatment with pramipexole dihydrochloride tablets, advise patients of the potential to develop drowsiness and specifically ask about factors that may increase the risk for somnolence with pramipexole dihydrochloride tablets such as the use of concomitant sedating medications or alcohol, the presence of sleep disorders, and concomitant medications that increase pramipexole plasma levels (e.g., cimetidine) [ see clinical pharmacology (12.3) ]. if a patient develops significant daytime sleepiness or episodes of falling asleep during activities that require active participation (e.g., conversations, eating, etc.), pramipexole dihydrochloride tablets should ordinarily be discontinued. if a decision is made to continue pramipexole dihydrochloride tablets, advise patients not to drive and to avoid other potentially dangerous activities that might result in harm if the patients become somnolent. while dose reduction reduces the degree of somnolence, there is insufficient information to establish that dose reduction will eliminate episodes of falling asleep while engaged in activities of daily living. 5.2 symptomatic orthostatic hypotension dopamine agonists, in clinical studies and clinical experience, appear to impair the systemic regulation of blood pressure, with resulting orthostatic hypotension, especially during dose escalation. parkinson's disease patients, in addition, appear to have an impaired capacity to respond to an orthostatic challenge. for these reasons, both parkinson's disease patients and rls patients being treated with dopaminergic agonists ordinarily require careful monitoring for signs and symptoms of orthostatic hypotension, especially during dose escalation, and should be informed of this risk. in clinical trials of pramipexole, however, and despite clear orthostatic effects in normal volunteers, the reported incidence of clinically significant orthostatic hypotension was not greater among those assigned to pramipexole tablets than among those assigned to placebo. this result, especially with the higher doses used in parkinson’s disease, is clearly unexpected in light of the previous experience with the risks of dopamine agonist therapy. while this finding could reflect a unique property of pramipexole, it might also be explained by the conditions of the study and the nature of the population enrolled in the clinical trials. patients were very carefully titrated, and patients with active cardiovascular disease or significant orthostatic hypotension at baseline were excluded. also, clinical trials in patients with rls did not incorporate orthostatic challenges with intensive blood pressure monitoring done in close temporal proximity to dosing. 5.3 impulse control/compulsive behaviors case reports and the results of a cross-sectional study suggest that patients can experience intense urges to gamble, increased sexual urges, intense urges to spend money uncontrollably, binge eating, and/or other intense urges and the inability to control these urges while taking one or more of the medications, including pramipexole dihydrochloride, that increase central dopaminergic tone. in some cases, although not all, these urges were reported to have stopped when the dose was reduced or the medication was discontinued. because patients may not recognize these behaviors as abnormal, it is important for prescribers to specifically ask patients or their caregivers about the development of new or increased gambling urges, sexual urges, uncontrolled spending or other urges while being treated with pramipexole dihydrochloride for parkinson's disease or rls. physicians should consider dose reduction or stopping the medication if a patient develops such urges while taking pramipexole dihydrochloride. 5.4 hallucinations and psychotic-like behavior in the three double-blind, placebo-controlled trials in early parkinson's disease, hallucinations were observed in 9% (35 of 388) of patients receiving pramipexole dihydrochloride tablets, compared with 2.6% (6 of 235) of patients receiving placebo. in the four double-blind, placebo-controlled trials in advanced parkinson's disease, where patients received pramipexole dihydrochloride tablets and concomitant levodopa, hallucinations were observed in 16.5% (43 of 260) of patients receiving pramipexole dihydrochloride tablets compared with 3.8% (10 of 264) of patients receiving placebo. hallucinations were of sufficient severity to cause discontinuation of treatment in 3.1% of the early parkinson's disease patients and 2.7% of the advanced parkinson's disease patients compared with about 0.4% of placebo patients in both populations. age appears to increase the risk of hallucinations attributable to pramipexole. in the early parkinson's disease patients, the risk of hallucinations was 1.9 times greater than placebo in patients younger than 65 years and 6.8 times greater than placebo in patients older than 65 years. in the advanced parkinson's disease patients, the risk of hallucinations was 3.5 times greater than placebo in patients younger than 65 years and 5.2 times greater than placebo in patients older than 65 years. postmarketing reports with medications used to treat parkinson’s disease or rls, including pramipexole dihydrochloride, indicate that patients may experience new or worsening mental status and behavioral changes, which may be severe, including psychotic-like behavior during treatment with pramipexole dihydrochloride or after starting or increasing the dose of pramipexole dihydrochloride. other drugs prescribed to improve the symptoms of parkinson’s disease or rls can have similar effects on thinking and behavior. this abnormal thinking and behavior can consist of one or more of a variety of manifestations including paranoid ideation, delusions, hallucinations, confusion, psychotic-like behavior, symptoms of mania (e.g., insomnia, psychomotor agitation), disorientation, aggressive behavior, agitation, and delirium. patients with a major psychotic disorder should ordinarily not be treated with dopamine agonists, including pramipexole dihydrochloride, because of the risk of exacerbating the psychosis. in addition, certain medications used to treat psychosis may exacerbate the symptoms of parkinson’s disease and may decrease the effectiveness of pramipexole dihydrochloride [ see drug interactions (7.1) ]. in the rls clinical trials, one pramipexole-treated patient (of 889) reported hallucinations; this patient discontinued treatment and the symptoms resolved. 5.5 dyskinesia pramipexole dihydrochloride tablets may cause or exacerbate preexisting dyskinesia. 5.6 postural deformity postural deformities, including antecollis, camptocormia (bent spine syndrome), and pleurothotonus (pisa syndrome), have been reported in patients after starting or increasing the dose of pramipexole dihydrochloride. postural deformity may occur several months after starting treatment or increasing the dose. reducing the dose or discontinuing pramipexole dihydrochloride has been reported to improve postural deformity in some patients, and should be considered if postural deformity occurs. 5.7 renal impairment since pramipexole is eliminated through the kidneys, caution should be exercised when prescribing pramipexole dihydrochloride tablets to patients with renal impairment [ see dosage and administration (2.3) , use in specific populations (8.6), and clinical pharmacology (12.3) ]. 5.8 rhabdomyolysis a single case of rhabdomyolysis occurred in a 49-year-old male with advanced parkinson's disease treated with pramipexole dihydrochloride tablets. the patient was hospitalized with an elevated cpk (10,631 iu/l). the symptoms resolved with discontinuation of the medication. advise patients to contact a physician if they experience any unexplained muscle pain, tenderness, or weakness, as these may be symptoms of rhabdomyolysis. 5.9 retinal pathology human data a two-year open-label, randomized, parallel-group safety study of retinal deterioration and vision compared pramipexole dihydrochloride tablets and immediate-release ropinirole. two hundred thirty four parkinson’s disease patients (115 on pramipexole, mean dose 3 mg/day and 119 on ropinirole, mean dose 9.5 mg/day) were evaluated using a panel of clinical ophthalmological assessments. of 234 patients who were evaluable, 196 had been treated for two years and 29 were judged to have developed clinical abnormalities that were considered meaningful (19 patients in each treatment arm had received treatment for less than two years). there was no statistical difference in retinal deterioration between the treatment arms; however, the study was only capable of detecting a very large difference between treatments. in addition, because the study did not include an untreated comparison group (placebo treated), it is unknown whether the findings reported in patients treated with either drug are greater than the background rate in an aging population. animal data pathologic changes (degeneration and loss of photoreceptor cells) were observed in the retina of albino rats in the 2-year carcinogenicity study. while retinal degeneration was not diagnosed in pigmented rats treated for 2 years, a thinning in the outer nuclear layer of the retina was slightly greater in rats given drug compared with controls. evaluation of the retinas of albino mice, monkeys, and minipigs did not reveal similar changes. the potential significance of this effect in humans has not been established, but cannot be disregarded because disruption of a mechanism that is universally present in vertebrates (i.e., disk shedding) may be involved [ see nonclinical toxicology (13.2) ]. 5.10 events reported with dopaminergic therapy although the events enumerated below may not have been reported in association with the use of pramipexole in its development program, they are associated with the use of other dopaminergic drugs. the expected incidence of these events, however, is so low that even if pramipexole caused these events at rates similar to those attributable to other dopaminergic therapies, it would be unlikely that even a single case would have occurred in a cohort of the size exposed to pramipexole in studies to date. hyperpyrexia and confusion although not reported with pramipexole in the clinical development program, a symptom complex resembling the neuroleptic malignant syndrome (characterized by elevated temperature, muscular rigidity, altered consciousness, and autonomic instability), with no other obvious etiology, has been reported in association with rapid dose reduction, withdrawal of, or changes in dopaminergic therapy. if possible, avoid sudden discontinuation or rapid dose reduction in patients taking pramipexole dihydrochloride tablets. if the decision is made to discontinue pramipexole dihydrochloride tablets, the dose should be tapered to reduce the risk of hyperpyrexia and confusion [ see dosage and administration (2.2) ]. fibrotic complications cases of retroperitoneal fibrosis, pulmonary infiltrates, pleural effusion, pleural thickening, pericarditis, and cardiac valvulopathy have been reported in patients treated with ergot-derived dopaminergic agents. while these complications may resolve when the drug is discontinued, complete resolution does not always occur. although these adverse events are believed to be related to the ergoline structure of these compounds, whether other, nonergot-derived dopamine agonists can cause them is unknown. cases of possible fibrotic complications, including peritoneal fibrosis, pleural fibrosis, and pulmonary fibrosis have been reported in the postmarketing experience with pramipexole dihydrochloride tablets. while the evidence is not sufficient to establish a causal relationship between pramipexole dihydrochloride tablets and these fibrotic complications, a contribution of pramipexole dihydrochloride tablets cannot be completely ruled out. rebound and augmentation in rls reports in the literature indicate treatment of rls with dopaminergic medications can result in rebound: a worsening of symptoms following treatment cessation with greater intensity than described before starting treatment. in a 26 week placebo-controlled clinical trial in patients with rls, a worsening of symptoms scores (irls) beyond their untreated baseline levels was reported more frequently by patients suddenly withdrawn from pramipexole dihydrochloride (up to 0.75 mg once daily) compared to the group assigned to placebo (10% vs. 2%, respectively). the worsening of rls symptoms was considered generally mild. augmentation has also been described during therapy for rls. augmentation refers to the earlier onset of symptoms in the evening (or even the afternoon), increase in symptoms, and spread of symptoms to involve other extremities. in a 26 week placebo-controlled clinical trial in patients with rls, augmentation was reported with greater frequency by patients treated with pramipexole dihydrochloride (up to 0.75 mg once daily) compared to patients who received placebo (12% vs. 9%, respectively). the incidence of augmentation increased with increasing duration of exposure to pramipexole dihydrochloride and to placebo. the frequency and severity of augmentation and/or rebound after longer-term use of pramipexole dihydrochloride tablets and the appropriate management of these events have not been adequately evaluated in controlled clinical trials. 5.11 withdrawal symptoms symptoms including apathy, anxiety, depression, fatigue, insomnia, sweating, and pain have been reported during taper or after discontinuation of dopamine agonists, including pramipexole dihydrochloride. these symptoms generally do not respond to levodopa. prior to discontinuation of pramipexole dihydrochloride, patients should be informed about potential withdrawal symptoms, and monitored during and after discontinuation. in case of severe withdrawal symptoms, a trial re-administration of a dopamine agonist at the lowest effective dose may be considered.

y with pramipexole dihydrochloride tablets has occurred, re-titration of therapy may be warranted. 2.2 dosing for parkinson's disease in all clinical studies, dosage was initiated at a subtherapeutic level to avoid intolerable adverse effects and orthostatic hypotension. pramipexole dihydrochloride tablets should be titrated gradually in all patients. the dose should be increased to achieve a maximum therapeutic effect, balanced against the principal side effects of dyskinesia, hallucinations, somnolence, and dry mouth. dosing in patients with normal renal function initial treatment doses should be increased gradually from a starting dose of 0.375 mg/day given in three divided doses and should not be increased more frequently than every 5 to 7 days. a suggested ascending dosage schedule that was used in clinical studies is shown in table 1: table 1 ascending dosage schedule of pramipexole dihydrochloride tablets for parkinson's disease week dosage (mg) total daily dose (mg) 1 0.125 three times a day 0.375 2 0.25 three times a day 0.75 3 0.5 three times a day 1.5 4 0.75 three times a day 2.25 5 1 three times a day 3 6 1.25 three times a day 3.75 7 1.5 three times a day 4.5 maintenance treatment pramipexole dihydrochloride tablets were effective and well tolerated over a dosage range of 1.5 to 4.5 mg/day administered in equally divided doses three times per day with or without concomitant levodopa (approximately 800 mg/day). in a fixed-dose study in early parkinson's disease patients, doses of 3 mg, 4.5 mg, and 6 mg per day of pramipexole dihydrochloride tablets were not shown to provide any significant benefit beyond that achieved at a daily dose of 1.5 mg/day. however, in the same fixed-dose study, the following adverse events were dose related: postural hypotension, nausea, constipation, somnolence, and amnesia. the frequency of these events was generally 2-fold greater than placebo for pramipexole doses greater than 3 mg/day. the incidence of somnolence reported with pramipexole at a dose of 1.5 mg/day was comparable to placebo. when pramipexole dihydrochloride tablets are used in combination with levodopa, a reduction of the levodopa dosage should be considered. in a controlled study in advanced parkinson's disease, the dosage of levodopa was reduced by an average of 27% from baseline. dosing in patients with renal impairment the recommended dosing of pramipexole dihydrochloride tablets in parkinson's disease patients with renal impairment is provided in table 2. table 2 dosing of pramipexole dihydrochloride tablets in parkinson’s disease patients with renal impairment renal status starting dose (mg) maximum dose (mg) normal to mild impairment (creatinine cl > 50 ml/min) 0.125 three times a day 1.5 three times a day moderate impairment (creatinine cl =30 to 50 ml/min) 0.125 twice a day 0.75 three times a day severe impairment (creatinine cl =15 to <30 ml/min) 0.125 once a day 1.5 once a day very severe impairment (creatinine cl <15 ml/min and hemodialysis patients) the use of pramipexole dihydrochloride tablets has not been adequately studied in this group of patients. discontinuation of treatment pramipexole dihydrochloride tablets may be tapered off at a rate of 0.75 mg per day until the daily dose has been reduced to 0.75 mg. thereafter, the dose may be reduced by 0.375 mg per day [see warnings and precautions (5.10 , 5.11) ] . 2.3 dosing for restless legs syndrome the recommended starting dose of pramipexole dihydrochloride tablets is 0.125 mg taken once daily 2 to 3 hours before bedtime. for patients requiring additional symptomatic relief, the dose may be increased every 4 to 7 days (table 3). although the dose of pramipexole dihydrochloride tablets was increased to 0.75 mg in some patients during long-term open-label treatment, there is no evidence that the 0.75 mg dose provides additional benefit beyond the 0.5 mg dose. table 3 ascending dosage schedule of pramipexole dihydrochloride tablets for rls *if needed titration step duration dose (mg) to be taken once daily, 2 to 3 hours before bedtime 1 4 to 7 days 0.125 2* 4 to 7 days 0.25 3* 4 to 7 days 0.5 dosing in patients with renal impairment the duration between titration steps should be increased to 14 days in rls patients with moderate and severe renal impairment (creatinine clearance 20 to 60 ml/min) [ see clinical pharmacology (12.3) ]. discontinuation of treatment in clinical trials of patients being treated for rls with doses up to 0.75 mg once daily, pramipexole dihydrochloride tablets were discontinued without a taper. in a 26 week placebo-controlled clinical trial, patients reported a worsening of rls symptom severity as compared to their untreated baseline when pramipexole dihydrochloride tablets treatment was suddenly withdrawn [see warnings and precautions (5.10) ] .

6.1) advanced pd with levodopa: postural (orthostatic) hypotension, dyskinesia, extrapyramidal syndrome, insomnia, dizziness, hallucinations, accidental injury, dream abnormalities, confusion, constipation, asthenia, somnolence, dystonia, gait abnormality, hypertonia, dry mouth, amnesia, and urinary frequency (6.1) rls: nausea, somnolence, fatigue, and headache ( 6.1 ) to report suspected adverse reactions, contact aurobindo pharma usa, inc. at 1-866-850-2876 or fda at 1-800-fda-1088 or www.fda.gov/medwatch . 6.1 clinical trials experience because clinical trials are conducted under widely varying conditions, adverse reaction rates observed in the clinical trials of a drug cannot be directly compared to rates in the clinical trials of another drug and may not reflect the rates observed in clinical practice. parkinson's disease during the premarketing development of pramipexole, patients with either early or advanced parkinson's disease were enrolled in clinical trials. apart from the severity and duration of their disease, the two populations differed in their use of concomitant levodopa therapy. patients with early disease did not receive concomitant levodopa therapy during treatment with pramipexole; those with advanced parkinson's disease all received concomitant levodopa treatment. because these two populations may have differential risks for various adverse reactions, this section will, in general, present adverse-reaction data for these two populations separately. because the controlled trials performed during premarketing development all used a titration design, with a resultant confounding of time and dose, it was impossible to adequately evaluate the effects of dose on the incidence of adverse reactions. early parkinson's disease in the three double-blind, placebo-controlled trials of patients with early parkinson's disease, the most common adverse reactions (>5%) that were numerically more frequent in the group treated with pramipexole dihydrochloride tablets were nausea, dizziness, somnolence, insomnia, constipation, asthenia, and hallucinations. approximately 12% of 388 patients with early parkinson's disease and treated with pramipexole dihydrochloride tablets who participated in the double-blind, placebo-controlled trials discontinued treatment due to adverse reactions compared with 11% of 235 patients who received placebo. the adverse reactions most commonly causing discontinuation of treatment were related to the nervous system (hallucinations [3.1% on pramipexole dihydrochloride tablets vs 0.4% on placebo]; dizziness [2.1% on pramipexole dihydrochloride tablets vs 1% on placebo]; somnolence [1.6% on pramipexole dihydrochloride tablets vs 0% on placebo]; headache and confusion [1.3% and 1.0%, respectively, on pramipexole dihydrochloride tablets vs 0% on placebo]) and gastrointestinal system (nausea [2.1% on pramipexole dihydrochloride tablets vs 0.4% on placebo]). adverse-reaction incidence in controlled clinical studies in early parkinson's disease: table 4 lists adverse reactions that occurred in the double-blind, placebo-controlled studies in early parkinson's disease that were reported by ?1% of patients treated with pramipexole dihydrochloride tablets and were numerically more frequent than in the placebo group. in these studies, patients did not receive concomitant levodopa. table 4 adverse-reactions in pooled double-blind, placebo-controlled trials with pramipexole dihydrochloride tablets in early parkinson’s disease body system/adverse reaction pramipexole dihydrochloride (n=388) % placebo (n=235) % nervous system dizziness 25 24 somnolence 22 9 insomnia 17 12 hallucinations 9 3 confusion 4 1 amnesia 4 2 hypesthesia 3 1 dystonia 2 1 akathisia 2 0 thinking abnormalities 2 0 decreased libido 1 0 myoclonus 1 0 digestive system nausea 28 18 constipation 14 6 anorexia 4 2 dysphagia 2 0 body as a whole asthenia 14 12 general edema 5 3 malaise 2 1 reaction unevaluable 2 1 fever 1 0 metabolic & nutritional system peripheral edema 5 4 decreased weight 2 0 special senses vision abnormalities 3 0 urogenital system impotence 2 1 in a fixed-dose study in early parkinson's disease, occurrence of the following reactions increased in frequency as the dose increased over the range from 1.5 mg/day to 6 mg/day: postural hypotension, nausea, constipation, somnolence, and amnesia. the frequency of these reactions was generally 2-fold greater than placebo for pramipexole doses greater than 3 mg/day. the incidence of somnolence with pramipexole at a dose of 1.5 mg/day was comparable to that reported for placebo. advanced parkinson's disease in the four double-blind, placebo-controlled trials of patients with advanced parkinson's disease, the most common adverse reactions (>5%) that were numerically more frequent in the group treated with pramipexole dihydrochloride tablets and concomitant levodopa were postural (orthostatic) hypotension, dyskinesia, extrapyramidal syndrome, insomnia, dizziness, hallucinations, accidental injury, dream abnormalities, confusion, constipation, asthenia, somnolence, dystonia, gait abnormality, hypertonia, dry mouth, amnesia, and urinary frequency. approximately 12% of 260 patients with advanced parkinson's disease who received pramipexole dihydrochloride tablets and concomitant levodopa in the double-blind, placebo-controlled trials discontinued treatment due to adverse reactions compared with 16% of 264 patients who received placebo and concomitant levodopa. the reactions most commonly causing discontinuation of treatment were related to the nervous system (hallucinations [2.7% on pramipexole dihydrochloride tablets vs 0.4% on placebo]; dyskinesia [1.9% on pramipexole dihydrochloride tablets vs 0.8% on placebo]) and cardiovascular system (postural [orthostatic] hypotension [2.3% on pramipexole dihydrochloride tablets vs 1.1% on placebo]). adverse-reaction incidence in controlled clinical studies in advanced parkinson's disease: table 5 lists adverse reactions that occurred in the double-blind, placebo-controlled studies in advanced parkinson's disease that were reported by ?1% of patients treated with pramipexole dihydrochloride tablets and were numerically more frequent than in the placebo group. in these studies, pramipexole dihydrochloride tablets or placebo was administered to patients who were also receiving concomitant levodopa. table 5 adverse-reactions in pooled double-blind, placebo-controlled trials with pramipexole dihydrochloride tablets in advanced parkinson's disease body system/adverse reaction pramipexole dihydrochloride (n=260) % placebo (n=264) % nervous system dyskinesia 47 31 extrapyramidal syndrome 28 26 insomnia 27 22 dizziness 26 25 hallucinations 17 4 dream abnormalities 11 10 confusion 10 7 somnolence 9 6 dystonia 8 7 gait abnormalities 7 5 hypertonia 7 6 amnesia 6 4 akathisia 3 2 thinking abnormalities 3 2 paranoid reaction 2 0 delusions 1 0 sleep disorders 1 0 cardiovascular system postural hypotension 53 48 body as a whole accidental injury 17 15 asthenia 10 8 general edema 4 3 chest pain 3 2 malaise 3 2 digestive system constipation 10 9 dry mouth 7 3 urogenital system urinary frequency 6 3 urinary tract infection 4 3 urinary incontinence 2 1 respiratory system dyspnea 4 3 rhinitis 3 1 pneumonia 2 0 special senses accommodation abnormalities 4 2 vision abnormalities 3 1 diplopia 1 0 musculoskeletal system arthritis 3 1 twitching 2 0 bursitis 2 0 myasthenia 1 0 metabolic & nutritional system peripheral edema 2 1 increased creatine pk 1 0 skin & appendages skin disorders 2 1 restless legs syndrome pramipexole dihydrochloride tablets for treatment of rls have been evaluated for safety in 889 patients, including 427 treated for over six months and 75 for over one year. the overall safety assessment focuses on the results of three double-blind, placebo-controlled trials, in which 575 patients with rls were treated with pramipexole dihydrochloride tablets for up to 12 weeks. the most common adverse reactions with pramipexole dihydrochloride tablets in the treatment of rls (observed in >5% of pramipexole-treated patients and at a rate at least twice that observed in placebo-treated patients) were nausea and somnolence. occurrences of nausea and somnolence in clinical trials were generally mild and transient. approximately 7% of 575 patients treated with pramipexole dihydrochloride tablets during the double-blind periods of three placebo-controlled trials discontinued treatment due to adverse reactions compared to 5% of 223 patients who received placebo. the adverse reaction most commonly causing discontinuation of treatment was nausea (1%). table 6 lists reactions that occurred in three double-blind, placebo-controlled studies in rls patients that were reported by ?2% of patients treated with pramipexole dihydrochloride tablets and were numerically more frequent than in the placebo group. table 6 adverse-reactions in pooled double-blind, placebo-controlled trials with pramipexole dihydrochloride tablets in restless legs syndrome body system/adverse reaction pramipexole dihydrochloride 0.125 to 0.75 mg/day (n=575) % placebo (n=223) % gastrointestinal disorders nausea 16 5 constipation 4 1 diarrhea 3 1 dry mouth 3 1 nervous system disorders headache 16 15 somnolence 6 3 general disorders and administration site conditions fatigue 9 7 infections and infestations influenza 3 1 table 7 summarizes data for adverse reactions that appeared to be dose related in the 12-week fixed dose study. table 7 dose-related adverse reactions in a 12-week double-blind, placebo-controlled fixed dose study in restless legs syndrome (occurring in ?5% of all patients in the treatment phase) body system/adverse reaction pramipexole dihydrochloride 0.25 mg (n=88) % pramipexole dihydrochloride 0.5 mg (n=80) % pramipexole dihydrochloride 0.75 mg (n=90) % placebo (n=86) % gastrointestinal disorders nausea 11 19 27 5 diarrhea 3 1 7 0 dyspepsia 3 1 4 7 psychiatric disorders insomnia 9 9 13 9 abnormal dreams 2 1 8 2 general disorders and administration site conditions fatigue 3 5 7 5 musculoskeletal and connective tissue disorders pain in extremity 3 3 7 1 infections and infestations influenza 1 4 7 1 respiratory, thoracic and mediastinal disorders nasal congestion 0 3 6 1 adverse reactions: relationship to age, gender, and race among the adverse reactions in patients treated with pramipexole dihydrochloride tablets, hallucination appeared to exhibit a positive relationship to age in patients with parkinson’s disease. although no gender-related differences were observed in parkinson’s disease patients, nausea and fatigue, both generally transient, were more frequently reported by female than male rls patients. less than 4% of patients enrolled were non-caucasian: therefore, an evaluation of adverse reactions related to race is not possible. laboratory tests during the development of pramipexole dihydrochloride tablets, no systematic abnormalities on routine laboratory testing were noted. 6.2 postmarketing experience in addition to the adverse events reported during clinical trials, the following adverse reactions have been identified during post-approval use of pramipexole dihydrochloride tablets, primarily in parkinson’s disease patients. because these reactions are reported voluntarily from a population of uncertain size, it is not always possible to reliably estimate their frequency or establish a causal relationship to drug exposure. decisions to include these reactions in labeling are typically based on one or more of the following factors: (1) seriousness of the reaction, (2) frequency of reporting, or (3) strength of causal connection to pramipexole tablets. cardiac disorders: cardiac failure gastrointestinal disorders: vomiting general disorders and administration site conditions : withdrawal symptoms [ see warnings and precautions (5.11) ] metabolism and nutrition disorders: syndrome of inappropriate antidiuretic hormone secretion (siadh), weight increase musculoskeletal and connective tissue disorders: postural deformity [see warnings and precautions (5.6) ] nervous system disorders: syncope skin and subcutaneous tissue disorders: skin reactions (including erythema, rash, pruritus, urticaria)

resorption of embryos at the highest dose tested. this increase in embryolethality is thought to result from the prolactin-lowering effect of pramipexole; prolactin is necessary for implantation and maintenance of early pregnancy in rats but not in rabbits or humans. because of pregnancy disruption and early embryonic loss in this study, the teratogenic potential of pramipexole could not be adequately assessed in rats. the highest no-effect dose for embryolethality in rats was associated with maternal plasma drug exposures (auc) approximately equal to those in humans receiving the maximum recommended human dose (mrhd) of 4.5 mg/day. there were no adverse effects on embryo-fetal development following oral administration of pramipexole (0.1, 1, or 10 mg/kg/day) to pregnant rabbits during organogenesis (plasma auc up to approximately 70 times that in humans at the mrhd). postnatal growth was inhibited in the offspring of rats treated with pramipexole (0.1, 0.5, or 1.5 mg/kg/day) during the latter part of pregnancy and throughout lactation. the no-effect dose for adverse effects on offspring growth (0.1 mg/kg/day) was associated with maternal plasma drug exposures lower than that in humans at the mrhd. 8.2 lactation risk summary there are no data on the presence of pramipexole in human milk, the effects of pramipexole on the breastfed infant, or the effects of pramipexole on milk production. however, inhibition of lactation is expected because pramipexole inhibits secretion of prolactin in humans. pramipexole or metabolites, or both, are present in rat milk [see data] . the developmental and health benefits of breastfeeding should be considered along with the mother’s clinical need for pramipexole dihydrochloride and any potential adverse effects on the breastfed infant from pramipexole dihydrochloride or from the underlying maternal condition. data in a study of radio-labeled pramipexole, pramipexole or metabolites, or both, were present in rat milk at concentrations three to six times higher than those in maternal plasma. 8.4 pediatric use safety and effectiveness of pramipexole dihydrochloride in pediatric patients has not been established. 8.5 geriatric use pramipexole total oral clearance is approximately 30% lower in subjects older than 65 years compared with younger subjects, because of a decline in pramipexole renal clearance due to an age-related reduction in renal function. this resulted in an increase in elimination half-life from approximately 8.5 hours to 12 hours. in clinical studies with parkinson’s disease patients, 38.7% of patients were older than 65 years. there were no apparent differences in efficacy or safety between older and younger patients, except that the relative risk of hallucination associated with the use of pramipexole dihydrochloride tablets was increased in the elderly. in clinical studies with rls patients, 22% of patients were at least 65 years old. there were no apparent differences in efficacy or safety between older and younger patients. 8.6 renal impairment the elimination of pramipexole is dependent on renal function. pramipexole clearance is extremely low in dialysis patients, as a negligible amount of pramipexole is removed by dialysis. caution should be exercised when administering pramipexole dihydrochloride tablets to patients with renal disease [ see dosage and administration (2.2), warnings and precautions (5.7) , and clinical pharmacology (12.3) ].

ught to result from the prolactin-lowering effect of pramipexole; prolactin is necessary for implantation and maintenance of early pregnancy in rats but not in rabbits or humans. because of pregnancy disruption and early embryonic loss in this study, the teratogenic potential of pramipexole could not be adequately assessed in rats. the highest no-effect dose for embryolethality in rats was associated with maternal plasma drug exposures (auc) approximately equal to those in humans receiving the maximum recommended human dose (mrhd) of 4.5 mg/day. there were no adverse effects on embryo-fetal development following oral administration of pramipexole (0.1, 1, or 10 mg/kg/day) to pregnant rabbits during organogenesis (plasma auc up to approximately 70 times that in humans at the mrhd). postnatal growth was inhibited in the offspring of rats treated with pramipexole (0.1, 0.5, or 1.5 mg/kg/day) during the latter part of pregnancy and throughout lactation. the no-effect dose for adverse effects on offspring growth (0.1 mg/kg/day) was associated with maternal plasma drug exposures lower than that in humans at the mrhd.

although the pathophysiology of rls is largely unknown, neuropharmacological evidence suggests primary dopaminergic system involvement. positron emission tomographic (pet) studies suggest that a mild striatal presynaptic dopaminergic dysfunction may be involved in the pathogenesis of rls. 12.2 pharmacodynamics the effect of pramipexole on the qt interval of the ecg was investigated in a clinical study in 60 healthy male and female volunteers. all subjects initiated treatment with 0.375 mg extended release pramipexole tablets administered once daily, and were up-titrated every 3 days to 2.25 mg and 4.5 mg daily, a faster rate of titration than recommended in the label. no dose- or exposure-related effect on mean qt intervals was observed; however, the study did not have a valid assessment of assay sensitivity. the effect of pramipexole on qtc intervals at higher exposures achieved either due to drug interactions (e.g., with cimetidine), renal impairment, or at higher doses has not been systematically evaluated. although mean values remained within normal reference ranges throughout the study, supine systolic blood pressure (sbp), diastolic blood pressure (dbp), and pulse rate for subjects treated with pramipexole generally increased during the rapid up-titration phase, by 10 mmhg, 7 mmhg, and 10 bpm higher than placebo, respectively. higher sbp, dbp, and pulse rates compared to placebo were maintained until the pramipexole doses were tapered; values on the last day of tapering were generally similar to baseline values. such effects have not been observed in clinical studies with parkinson’s disease patients, who were titrated according to labeled recommendations. 12.3 pharmacokinetics pramipexole displays linear pharmacokinetics over the clinical dosage range. its terminal half-life is about 8 hours in young healthy volunteers and about 12 hours in elderly volunteers. steady-state concentrations are achieved within 2 days of dosing. absorption pramipexole is rapidly absorbed, reaching peak concentrations in approximately 2 hours. the absolute bioavailability of pramipexole is greater than 90%, indicating that it is well absorbed and undergoes little presystemic metabolism. food does not affect the extent of pramipexole absorption, although the time of maximum plasma concentration (t max ) is increased by about 1 hour when the drug is taken with a meal. distribution pramipexole is extensively distributed, having a volume of distribution of about 500 l (coefficient of variation [cv]=20%). it is about 15% bound to plasma proteins. pramipexole distributes into red blood cells as indicated by an erythrocyte-to-plasma ratio of approximately 2. metabolism pramipexole is metabolized only to a negligible extent (<10%). no specific active metabolite has been identified in human plasma or urine. elimination urinary excretion is the major route of pramipexole elimination, with 90% of a pramipexole dose recovered in urine, almost all as unchanged drug. the renal clearance of pramipexole is approximately 400 ml/min (cv=25%), approximately three times higher than the glomerular filtration rate. thus, pramipexole is secreted by the renal tubules, probably by the organic cation transport system. pharmacokinetics in specific populations because therapy with pramipexole dihydrochloride tablets is initiated at a low dose and gradually titrated upward according to clinical tolerability to obtain the optimum therapeutic effect, adjustment of the initial dose based on gender, weight, race, or age is not necessary. however, renal insufficiency, which can cause a large decrease in the ability to eliminate pramipexole, may necessitate dosage adjustment [ see dosage and administration (2.2) ]. gender pramipexole clearance is about 30% lower in women than in men, but this difference can be accounted for by differences in body weight. there is no difference in half-life between males and females. age pramipexole clearance decreases with age as the half-life and clearance are about 40% longer and 30% lower, respectively, in elderly (aged 65 years or older) compared with young healthy volunteers (aged less than 40 years). this difference is most likely due to the reduction in renal function with age, since pramipexole clearance is correlated with renal function, as measured by creatinine clearance. race no racial differences in metabolism and elimination have been identified. parkinson's disease patients a cross-study comparison of data suggests that the clearance of pramipexole may be reduced by about 30% in parkinson's disease patients compared with healthy elderly volunteers. the reason for this difference appears to be reduced renal function in parkinson's disease patients, which may be related to their poorer general health. the pharmacokinetics of pramipexole were comparable between early and advanced parkinson's disease patients. restless legs syndrome patients a cross-study comparison of data suggests that the pharmacokinetic profile of pramipexole administered once daily in rls patients is similar to the pharmacokinetic profile of pramipexole in healthy volunteers. hepatic impairment the influence of hepatic insufficiency on pramipexole pharmacokinetics has not been evaluated. because approximately 90% of the recovered dose is excreted in the urine as unchanged drug, hepatic impairment would not be expected to have a significant effect on pramipexole elimination. renal impairment clearance of pramipexole was about 75% lower in patients with severe renal impairment (creatinine clearance approximately 20 ml/min) and about 60% lower in patients with moderate impairment (creatinine clearance approximately 40 ml/min) compared with healthy volunteers [ see warnings and precautions (5.7) and dosage and administration (2.2) ]. in patients with varying degrees of renal impairment, pramipexole clearance correlates well with creatinine clearance. therefore, creatinine clearance can be used as a predictor of the extent of decrease in pramipexole clearance. drug interactions carbidopa/levodopa: carbidopa/levodopa did not influence the pharmacokinetics of pramipexole in healthy volunteers (n=10). pramipexole did not alter the extent of absorption (auc) or the elimination of carbidopa/levodopa, although it caused an increase in levodopa c max by about 40% and a decrease in t max from 2.5 to 0.5 hours. selegiline: in healthy volunteers (n=11), selegiline did not influence the pharmacokinetics of pramipexole. amantadine: population pharmacokinetic analyses suggest that amantadine may slightly decrease the oral clearance of pramipexole. cimetidine: cimetidine, a known inhibitor of renal tubular secretion of organic bases via the cationic transport system, caused a 50% increase in pramipexole auc and a 40% increase in half-life (n=12). probenecid: probenecid, a known inhibitor of renal tubular secretion of organic acids via the anionic transporter, did not noticeably influence pramipexole pharmacokinetics (n=12). other drugs eliminated via renal secretion: population pharmacokinetic analysis suggests that coadministration of drugs that are secreted by the cationic transport system (e.g., cimetidine, ranitidine, diltiazem, triamterene, verapamil, quinidine, and quinine) decreases the oral clearance of pramipexole by about 20%, while those secreted by the anionic transport system (e.g., cephalosporins, penicillins, indomethacin, hydrochlorothiazide, and chlorpropamide) are likely to have little effect on the oral clearance of pramipexole. other known organic cation transport substrates and/or inhibitors (e.g., cisplatin and procainamide) may also decrease the clearance of pramipexole. cyp interactions: inhibitors of cytochrome p450 enzymes would not be expected to affect pramipexole elimination because pramipexole is not appreciably metabolized by these enzymes in vivo or in vitro . pramipexole does not inhibit cyp enzymes cyp1a2, cyp2c9, cyp2c19, cyp2e1, and cyp3a4. inhibition of cyp2d6 was observed with an apparent ki of 30 ?m, indicating that pramipexole will not inhibit cyp enzymes at plasma concentrations observed following the clinical dose of 4.5 mg/day (1.5 mg tid).

lism pramipexole is metabolized only to a negligible extent (<10%). no specific active metabolite has been identified in human plasma or urine. elimination urinary excretion is the major route of pramipexole elimination, with 90% of a pramipexole dose recovered in urine, almost all as unchanged drug. the renal clearance of pramipexole is approximately 400 ml/min (cv=25%), approximately three times higher than the glomerular filtration rate. thus, pramipexole is secreted by the renal tubules, probably by the organic cation transport system. pharmacokinetics in specific populations because therapy with pramipexole dihydrochloride tablets is initiated at a low dose and gradually titrated upward according to clinical tolerability to obtain the optimum therapeutic effect, adjustment of the initial dose based on gender, weight, race, or age is not necessary. however, renal insufficiency, which can cause a large decrease in the ability to eliminate pramipexole, may necessitate dosage adjustment [ see dosage and administration (2.2) ]. gender pramipexole clearance is about 30% lower in women than in men, but this difference can be accounted for by differences in body weight. there is no difference in half-life between males and females. age pramipexole clearance decreases with age as the half-life and clearance are about 40% longer and 30% lower, respectively, in elderly (aged 65 years or older) compared with young healthy volunteers (aged less than 40 years). this difference is most likely due to the reduction in renal function with age, since pramipexole clearance is correlated with renal function, as measured by creatinine clearance. race no racial differences in metabolism and elimination have been identified. parkinson's disease patients a cross-study comparison of data suggests that the clearance of pramipexole may be reduced by about 30% in parkinson's disease patients compared with healthy elderly volunteers. the reason for this difference appears to be reduced renal function in parkinson's disease patients, which may be related to their poorer general health. the pharmacokinetics of pramipexole were comparable between early and advanced parkinson's disease patients. restless legs syndrome patients a cross-study comparison of data suggests that the pharmacokinetic profile of pramipexole administered once daily in rls patients is similar to the pharmacokinetic profile of pramipexole in healthy volunteers. hepatic impairment the influence of hepatic insufficiency on pramipexole pharmacokinetics has not been evaluated. because approximately 90% of the recovered dose is excreted in the urine as unchanged drug, hepatic impairment would not be expected to have a significant effect on pramipexole elimination. renal impairment clearance of pramipexole was about 75% lower in patients with severe renal impairment (creatinine clearance approximately 20 ml/min) and about 60% lower in patients with moderate impairment (creatinine clearance approximately 40 ml/min) compared with healthy volunteers [ see warnings and precautions (5.7) and dosage and administration (2.2) ]. in patients with varying degrees of renal impairment, pramipexole clearance correlates well with creatinine clearance. therefore, creatinine clearance can be used as a predictor of the extent of decrease in pramipexole clearance. drug interactions carbidopa/levodopa: carbidopa/levodopa did not influence the pharmacokinetics of pramipexole in healthy volunteers (n=10). pramipexole did not alter the extent of absorption (auc) or the elimination of carbidopa/levodopa, although it caused an increase in levodopa c max by about 40% and a decrease in t max from 2.5 to 0.5 hours. selegiline: in healthy volunteers (n=11), selegiline did not influence the pharmacokinetics of pramipexole. amantadine: population pharmacokinetic analyses suggest that amantadine may slightly decrease the oral clearance of pramipexole. cimetidine: cimetidine, a known inhibitor of renal tubular secretion of organic bases via the cationic transport system, caused a 50% increase in pramipexole auc and a 40% increase in half-life (n=12). probenecid: probenecid, a known inhibitor of renal tubular secretion of organic acids via the anionic transporter, did not noticeably influence pramipexole pharmacokinetics (n=12). other drugs eliminated via renal secretion: population pharmacokinetic analysis suggests that coadministration of drugs that are secreted by the cationic transport system (e.g., cimetidine, ranitidine, diltiazem, triamterene, verapamil, quinidine, and quinine) decreases the oral clearance of pramipexole by about 20%, while those secreted by the anionic transport system (e.g., cephalosporins, penicillins, indomethacin, hydrochlorothiazide, and chlorpropamide) are likely to have little effect on the oral clearance of pramipexole. other known organic cation transport substrates and/or inhibitors (e.g., cisplatin and procainamide) may also decrease the clearance of pramipexole. cyp interactions: inhibitors of cytochrome p450 enzymes would not be expected to affect pramipexole elimination because pramipexole is not appreciably metabolized by these enzymes in vivo or in vitro . pramipexole does not inhibit cyp enzymes cyp1a2, cyp2c9, cyp2c19, cyp2e1, and cyp3a4. inhibition of cyp2d6 was observed with an apparent ki of 30 ?m, indicating that pramipexole will not inhibit cyp enzymes at plasma concentrations observed following the clinical dose of 4.5 mg/day (1.5 mg tid).

ated with reductions in serum levels of prolactin, a hormone necessary for implantation and maintenance of early pregnancy in rats. 13.2 animal toxicology and/or pharmacology retinal pathology in rats pathologic changes (degeneration and loss of photoreceptor cells) were observed in the retina of albino rats in the 2-year carcinogenicity study with pramipexole. these findings were first observed during week 76 and were dose-dependent in animals receiving 2 or 8 mg/kg/day (plasma aucs equal to 2.5 and 12.5 times that in humans at the mrhd). in a similar study of pigmented rats with 2 years exposure to pramipexole at 2 or 8 mg/kg/day, retinal degeneration was not observed. animals given drug had thinning in the outer nuclear layer of the retina that was only slightly greater (by morphometric analysis) than that seen in control rats. investigative studies demonstrated that pramipexole reduced the rate of disk shedding from the photoreceptor rod cells of the retina in albino rats, which was associated with enhanced sensitivity to the damaging effects of light. in a comparative study, degeneration and loss of photoreceptor cells occurred in albino rats after 13 weeks of treatment with 25 mg/kg/day of pramipexole (54 times the mrhd on a mg/m 2 basis) and constant light (100 lux) but not in pigmented rats exposed to the same dose and higher light intensities (500 lux). thus, the retina of albino rats is considered to be uniquely sensitive to the damaging effects of pramipexole and light. similar changes in the retina did not occur in a 2-year carcinogenicity study in albino mice treated with 0.3, 2, or 10 mg/kg/day (0.3, 2.2 and 11 times the mrhd on a mg/m 2 basis). evaluation of the retinas of monkeys given 0.1, 0.5, or 2 mg/kg/day of pramipexole (0.4, 2.2, and 8.6 times the mrhd on a mg/m 2 basis) for 12 months and minipigs given 0.3, 1, or 5 mg/kg/day of pramipexole for 13 weeks also detected no changes. the potential significance of this effect in humans has not been established, but cannot be disregarded because disruption of a mechanism that is universally present in vertebrates (i.e., disk shedding) may be involved. fibro-osseous proliferative lesions in mice an increased incidence of fibro-osseous proliferative lesions occurred in the femurs of female mice treated for 2 years with 0.3, 2, or 10 mg/kg/day (0.3, 2.2, and 11 times the mrhd on a mg/m 2 basis). similar lesions were not observed in male mice or rats and monkeys of either sex that were treated chronically with pramipexole. the significance of this lesion to humans is not known.

rum levels of prolactin, a hormone necessary for implantation and maintenance of early pregnancy in rats.

subparts, served as the primary outcome assessment measure. the updrs is a four-part multi-item rating scale intended to evaluate mentation (part i), activities of daily living (adl) (part ii), motor performance (part iii), and complications of therapy (part iv). part ii of the updrs contains 13 questions relating to adl, which are scored from 0 (normal) to 4 (maximal severity) for a maximum (worst) score of 52. part iii of the updrs contains 27 questions (for 14 items) and is scored as described for part ii. it is designed to assess the severity of the cardinal motor findings in patients with parkinson's disease (e.g., tremor, rigidity, bradykinesia, postural instability, etc.), scored for different body regions, and has a maximum (worst) score of 108. studies in patients with early parkinson's disease patients (n=599) in the two studies of early parkinson's disease had a mean disease duration of 2 years, limited or no prior exposure to levodopa (generally none in the preceding 6 months), and were not experiencing the "on-off" phenomenon and dyskinesia characteristic of later stages of the disease. one of the two early parkinson's disease studies (n=335) was a double-blind, placebo-controlled, parallel trial consisting of a 7-week dose-escalation period and a 6-month maintenance period. patients could be on selegiline, anticholinergics, or both, but could not be on levodopa products or amantadine. patients were randomized to pramipexole dihydrochloride tablets or placebo. patients treated with pramipexole dihydrochloride tablets had a starting daily dose of 0.375 mg and were titrated to a maximally tolerated dose, but no higher than 4.5 mg/day in three divided doses. at the end of the 6-month maintenance period, the mean improvement from baseline on the updrs part ii (adl) total score was 1.9 in the group receiving pramipexole dihydrochloride tablets and -0.4 in the placebo group, a difference that was statistically significant. the mean improvement from baseline on the updrs part iii total score was 5.0 in the group receiving pramipexole dihydrochloride tablets and -0.8 in the placebo group, a difference that was also statistically significant. a statistically significant difference between groups in favor of pramipexole dihydrochloride tablets was seen beginning at week 2 of the updrs part ii (maximum dose 0.75 mg/day) and at week 3 of the updrs part iii (maximum dose 1.5 mg/day). the second early parkinson's disease study (n=264) was a double-blind, placebo-controlled, parallel trial consisting of a 6-week dose-escalation period and a 4-week maintenance period. patients could be on selegiline, anticholinergics, amantadine, or any combination of these, but could not be on levodopa products. patients were randomized to 1 of 4 fixed doses of pramipexole dihydrochloride tablets (1.5 mg, 3 mg, 4.5 mg, or 6 mg per day) or placebo. at the end of the 4-week maintenance period, the mean improvement from baseline on the updrs part ii total score was 1.8 in the patients treated with pramipexole dihydrochloride tablets, regardless of assigned dose group, and 0.3 in placebo-treated patients. the mean improvement from baseline on the updrs part iii total score was 4.2 in patients treated with pramipexole dihydrochloride tablets and 0.6 in placebo-treated patients. no dose-response relationship was demonstrated. the between-treatment differences on both parts of the updrs were statistically significant in favor of pramipexole dihydrochloride tablets for all doses. no differences in effectiveness based on age or gender were detected. there were too few non-caucasian patients to evaluate the effect of race. patients receiving selegiline or anticholinergics had responses similar to patients not receiving these drugs. studies in patients with advanced parkinson's disease in the advanced parkinson's disease study, the primary assessments were the updrs and daily diaries that quantified amounts of "on" and "off" time. patients in the advanced parkinson's disease study (n=360) had a mean disease duration of 9 years, had been exposed to levodopa for long periods of time (mean 8 years), used concomitant levodopa during the trial, and had "on-off" periods. the advanced parkinson's disease study was a double-blind, placebo-controlled, parallel trial consisting of a 7-week dose-escalation period and a 6-month maintenance period. patients were all treated with concomitant levodopa products and could additionally be on concomitant selegiline, anticholinergics, amantadine, or any combination. patients treated with pramipexole dihydrochloride tablets had a starting dose of 0.375 mg/day and were titrated to a maximally tolerated dose, but no higher than 4.5 mg/day in three divided doses. at selected times during the 6-month maintenance period, patients were asked to record the amount of "off," "on," or "on with dyskinesia" time per day for several sequential days. at the end of the 6-month maintenance period, the mean improvement from baseline on the updrs part ii total score was 2.7 in the group treated with pramipexole dihydrochloride tablets and 0.5 in the placebo group, a difference that was statistically significant. the mean improvement from baseline on the updrs part iii total score was 5.6 in the group treated with pramipexole dihydrochloride tablets and 2.8 in the placebo group, a difference that was statistically significant. a statistically significant difference between groups in favor of pramipexole dihydrochloride tablets was seen at week 3 of the updrs part ii (maximum dose 1.5 mg/day) and at week 2 of the updrs part iii (maximum dose 0.75 mg/day). dosage reduction of levodopa was allowed during this study if dyskinesia (or hallucinations) developed; levodopa dosage reduction occurred in 76% of patients treated with pramipexole dihydrochloride tablets versus 54% of placebo patients. on average, the levodopa dose was reduced 27%. the mean number of "off" hours per day during baseline was 6 hours for both treatment groups. throughout the trial, patients treated with pramipexole dihydrochloride tablets had a mean of 4 "off" hours per day, while placebo-treated patients continued to experience 6 "off" hours per day. no differences in effectiveness based on age or gender were detected. there were too few non-caucasian patients to evaluate the effect of race. 14.2 restless legs syndrome the efficacy of pramipexole dihydrochloride tablets in the treatment of rls was evaluated in a multinational drug development program consisting of 4 randomized, double-blind, placebo-controlled trials. this program included approximately 1000 patients with moderate to severe rls; patients with rls secondary to other conditions (e.g., pregnancy, renal failure, and anemia) were excluded. all patients were administered pramipexole dihydrochloride tablets (0.125 mg, 0.25 mg, 0.5 mg, or 0.75 mg) or placebo once daily 2 to 3 hours before going to bed. across the 4 studies, the mean duration of rls was 4.6 years (range of 0 to 56 years), mean age was approximately 55 years (range of 18 to 81 years), and approximately 66.6% were women. key diagnostic criteria for rls are: an urge to move the legs usually accompanied or caused by uncomfortable and unpleasant leg sensations; symptoms begin or worsen during periods of rest or inactivity such as lying or sitting; symptoms are partially or totally relieved by movement such as walking or stretching at least as long as the activity continues; and symptoms are worse or occur only in the evening or night. difficulty falling asleep may frequently be associated with symptoms of rls. the two outcome measures used to assess the effect of treatment were the international rls rating scale (irls scale) and a clinical global impression - improvement (cgi-i) assessment. the irls scale contains 10 items designed to assess the severity of sensory and motor symptoms, sleep disturbance, daytime somnolence, and impact on activities of daily living and mood associated with rls. the range of scores is 0 to 40, with 0 being absence of rls symptoms and 40 the most severe symptoms. the cgi-i is designed to assess clinical progress (global improvement) on a 7-point scale. in study 1, fixed doses of pramipexole dihydrochloride tablets were compared to placebo in a study of 12 weeks duration. a total of 344 patients were randomized equally to the 4 treatment groups. patients treated with pramipexole dihydrochloride tablets (n=254) had a starting dose of 0.125 mg/day and were titrated to one of the three randomized doses (0.25, 0.5, 0.75 mg/day) in the first three weeks of the study. the mean improvement from baseline on the irls scale total score and the percentage of cgi-i responders for each of the pramipexole dihydrochloride tablets treatment groups compared to placebo are summarized in table 8. all treatment groups reached statistically significant superiority compared to placebo for both endpoints. there was no clear evidence of a dose-response across the 3 randomized dose groups. table 8 mean changes from baseline to week 12 in irls score and cgi-i (study 1) pramipexole dihydrochloride 0.25 mg pramipexole dihydrochloride 0.5 mg pramipexole dihydrochloride 0.75 mg pramipexole dihydrochloride total placebo no. patients 88 79 87 254 85 irls score -13.1 -13.4 -14.4 -13.6 -9.4 cgi-i responders* 74.7% 67.9% 72.9% 72.0% 51.2% *cgi-i responders = “much improved” and “very much improved” study 2 was a randomized-withdrawal study, designed to demonstrate the sustained efficacy of pramipexole for treatment of rls after a period of six months. rls patients who responded to pramipexole dihydrochloride tablets treatment in a preceding 6-month open-label treatment phase (defined as having a cgi-i rating of “very much improved” or “much improved” compared to baseline and an irls score of 15 or below) were randomized to receive either continued active treatment (n=78) or placebo (n=69) for 12 weeks. the primary endpoint of this study was time to treatment failure, defined as any worsening on the cgi-i score along with an irls scale total score above 15. in patients who had responded to 6-month open label treatment with pramipexole dihydrochloride tablets, the administration of placebo led to a rapid decline in their overall conditions and return of their rls symptoms. at the end of the 12-week observation period, 85% of patients treated with placebo had failed treatment, compared to 21% treated with blinded pramipexole, a difference that was highly statistically significant. the majority of treatment failures occurred within 10 days of randomization. for the patients randomized, the distribution of doses was: 7 on 0.125 mg, 44 on 0.25 mg, 47 on 0.5 mg, and 49 on 0.75 mg. study 3 was a 6-week study, comparing a flexible dose of pramipexole dihydrochloride tablets to placebo. in this study, 345 patients were randomized in a 2:1 ratio to pramipexole dihydrochloride tablets or placebo. the mean improvement from baseline on the irls scale total score was -12 for pramipexole dihydrochloride-treated patients and -6 for placebo-treated patients. the percentage of cgi-i responders was 63% for pramipexole dihydrochloride-treated patients and 32% for placebo-treated patients. the between-group differences were statistically significant for both outcome measures. for the patients randomized to pramipexole dihydrochloride tablets, the distribution of achieved doses was: 35 on 0.125 mg, 51 on 0.25 mg, 65 on 0.5 mg, and 69 on 0.75 mg. study 4 was a 3-week study, comparing 4 fixed doses of pramipexole dihydrochloride tablets, 0.125 mg, 0.25 mg, 0.5 mg, and 0.75 mg, to placebo. approximately 20 patients were randomized to each of the 5 dose groups. the mean improvement from baseline on the irls scale total score and the percentage of cgi-i responders for each of the pramipexole dihydrochloride tablets treatment groups compared to placebo are summarized in table 9. in this study, the 0.125 mg dose group was not significantly different from placebo. on average, the 0.5 mg dose group performed better than the 0.25 mg dose group, but there was no difference between the 0.5 mg and 0.75 mg dose groups. table 9 mean changes from baseline to week 3 in irls score and cgi-i (study 4) pramipexole dihydrochloride 0.125 mg pramipexole dihydrochloride 0.25 mg pramipexole dihydrochloride 0.5 mg pramipexole dihydrochloride 0.75 mg pramipexole dihydrochloride total placebo no. patients 21 22 22 21 86 21 irls score -11.7 -15.3 -17.6 -15.2 -15.0 -6.2 cgi-i responders* 61.9% 68.2% 86.4% 85.7% 75.6% 42.9% *cgi-i responders = “much improved” and “very much improved” no differences in effectiveness based on age or gender were detected. there were too few non-caucasian patients to evaluate the effect of race.

c 65862-606-90 bottles of 1,000 ndc 65862-606-99 cartons of 100 (10 x 10) unit-dose tablets ndc 65862-606-78 pramipexole dihydrochloride tablets, 0.75 mg are white to off-white, oval, biconcave, beveled edge uncoated tablets, debossed with ‘y’ on one side and ‘44’ on other side. bottles of 90 ndc 65862-607-90 bottles of 1,000 ndc 65862-607-99 cartons of 100 (10 x 10) unit-dose tablets ndc 65862-607-78 pramipexole dihydrochloride tablets, 1 mg are white to off-white, round, flat, beveled edge uncoated tablets, debossed with ‘y’ and ‘45’ separated by score line on one side and plain with score line on other side. bottles of 90 ndc 65862-608-90 bottles of 1,000 ndc 65862-608-99 cartons of 100 (10 x 10) unit-dose tablets ndc 65862-608-78 pramipexole dihydrochloride tablets, 1.5 mg are white to off-white, round, flat, beveled edge uncoated tablets, debossed with ‘y’ and ‘46’ separated by score line on one side and plain with score line on other side. bottles of 90 ndc 65862-609-90 bottles of 1,000 ndc 65862-609-99 cartons of 100 (10 x 10) unit-dose tablets ndc 65862-609-78 16.2 storage and handling store at 20° to 25°c (68° to 77°f) [see usp controlled room temperature]. protect from light. store in a safe place out of the reach of children.

tentially serious consequences, patients should neither drive a car nor engage in other potentially dangerous activities until they have gained sufficient experience with pramipexole dihydrochloride tablets to gauge whether or not it affects their mental and/or motor performance adversely. advise patients that if increased somnolence or new episodes of falling asleep during activities of daily living (e.g., conversations or eating) are experienced at any time during treatment, they should not drive or participate in potentially dangerous activities until they have contacted their physician. because of possible additive effects, advise caution when patients are taking other sedating medications or alcohol in combination with pramipexole dihydrochloride tablets and when taking concomitant medications that increase plasma levels of pramipexole (e.g., cimetidine) [ see warnings and precautions (5.1) ] . postural (orthostatic) hypotension advise patients that they may develop postural (orthostatic) hypotension, with or without symptoms such as dizziness, nausea, fainting or blackouts, and sometimes, sweating. hypotension may occur more frequently during initial therapy. accordingly, caution patients against rising rapidly after sitting or lying down, especially if they have been doing so for prolonged periods and especially at the initiation of treatment with pramipexole dihydrochloride tablets [ see warnings and precautions (5.2) ]. impulse control symptoms including compulsive behaviors alert patients and their caregivers to the possibility that they may experience intense urges to spend money uncontrollably, intense urges to gamble, increased sexual urges, binge eating and/or other intense urges and the inability to control these urges while taking pramipexole dihydrochloride [ see warnings and precautions (5.3) ]. hallucinations and psychotic-like behavior inform patients that hallucinations and other psychotic-like behavior can occur. in patients with parkinson's disease, the elderly are at a higher risk than younger patients [ see warnings and precautions (5.4) ]. withdrawal-emergent hyperpyrexia and confusion advise patients who have been prescribed a lower dose or who have been withdrawn from the drug to notify their healthcare provider if they have symptoms such as fever, muscular rigidity, or altered consciousness [ see warnings and precautions (5.10) ]. withdrawal symptoms advise patients that withdrawal symptoms may occur during or after discontinuation or dose reduction of pramipexole dihydrochloride. advise patients who have been prescribed a lower dose or who have been withdrawn from the drug to notify their healthcare provider if they have withdrawal symptoms such as apathy, anxiety, depression, fatigue, insomnia, sweating, or pain. notify patients that in case of severe withdrawal symptoms, a trial re-administration of a dopamine agonist at the lowest effective dose may be considered [ see warnings and precautions (5.11) ]. pregnancy because the teratogenic potential of pramipexole has not been completely established in laboratory animals, and because experience in humans is limited, advise women to notify their physicians if they become pregnant or intend to become pregnant during therapy [ see use in specific populations (8.1) ]. lactation because of the possibility that pramipexole may be excreted in breast milk, advise women to notify their physicians if they intend to breast-feed or are breast-feeding an infant [ see use in specific populations (8.2) ]. distributed by: aurobindo pharma usa, inc. 279 princeton-hightstown road east windsor, nj 08520 manufactured by: aurobindo pharma limited hyderabad-500 032, india revised: 07/2021

etting up from sitting or lying down have trouble controlling your muscles (dyskinesia) have kidney problems drink alcohol. alcohol can increase the chance that pramipexole dihydrochloride tablets will make you feel sleepy or fall asleep when you should be awake. have any other medical conditions are pregnant or plan to become pregnant. it is not known if pramipexole dihydrochloride tablets will harm your unborn baby. are breastfeeding or plan to breastfeed. it is not known if pramipexole dihydrochloride passes into your breast milk. you and your doctor should decide if you will take pramipexole dihydrochloride tablets or breastfeed. you should not do both. tell your doctor about all the medicines you take, including prescription and non-prescription medicines, vitamins, and herbal supplements. the combination of pramipexole dihydrochloride tablets and other medicines may affect each other and may cause side effects. pramipexole dihydrochloride tablets may affect the way other medicines work, and other medicines may affect how pramipexole dihydrochloride tablet works. especially tell your doctor if you take: medicines called neuroleptics (phenothiazines, butyrophenones, thioxanthenes) or metoclopramide. pramipexole dihydrochloride tablets may not work as well if you take these medicines. pramipexole dihydrochloride extended-release tablets. pramipexole is the active ingredient in both pramipexole dihydrochloride tablets and pramipexole dihydrochloride extended-release tablets. if you are taking pramipexole dihydrochloride extended-release tablets, you should not take pramipexole dihydrochloride tablets. any other medicines that make you sleepy or may increase the effects of pramipexole dihydrochloride tablets, such as cimetidine (tagamet). ask your doctor for a list of these medicines if you are not sure. know the medicines you take. keep a list of them and show it to your doctor and pharmacist when you get a new medicine. how should i take pramipexole dihydrochloride tablets? take pramipexole dihydrochloride tablets exactly as your doctor tells you to take them. your doctor will tell you how much pramipexole dihydrochloride to take and when to take it. do not take more or less pramipexole dihydrochloride tablets than your doctor tells you to. your doctor may change your dose if needed. pramipexole dihydrochloride tablets can be taken with or without food. taking pramipexole dihydrochloride tablets with food may lower your chances of getting nausea. if you take more pramipexole dihydrochloride tablets than your doctor recommends, call your doctor or go to the nearest hospital emergency room right away. if you miss a dose, do not double your next dose . skip the dose you missed and take your next regular dose. do not stop taking pramipexole dihydrochloride tablets without talking to your doctor first. if your doctor tells you to stop taking pramipexole dihydrochloride tablets, you should ask your doctor for specific instructions on how to safely discontinue taking pramipexole dihydrochloride tablets. if you stop pramipexole dihydrochloride tablets you may have withdrawal symptoms (see “withdrawal symptoms” under “what are the possible side effects of pramipexole dihydrochloride tablets?” ). what should i avoid while taking pramipexole dihydrochloride tablets ? do not drink alcohol while taking pramipexole dihydrochloride tablets. it can increase your chance of having serious side effects. see “what are the possible side effects of pramipexole dihydrochloride tablets?” do not drive a car, operate a machine, or do other dangerous activities until you know how pramipexole dihydrochloride tablets affect you. sleepiness caused by pramipexole dihydrochloride tablets can happen as late as 1 year after you start your treatment. what are the possible side effects of pramipexole dihydrochloride tablets ? pramipexole dihydrochloride tablets may cause serious side effects, including: falling asleep during normal daily activities . pramipexole dihydrochloride tablets may cause you to fall asleep while you are doing daily activities such as driving, talking with other people, or eating. some people taking the medicine in pramipexole dihydrochloride tablets have had car accidents because they fell asleep while driving. some patients did not feel sleepy before they fell asleep while driving. you could fall asleep without any warning. tell your doctor right away if you fall asleep while you are doing activities such as talking, eating, driving, or if you feel sleepier than normal for you. low blood pressure when you sit or stand up quickly. you may have: dizziness nausea fainting sweating sit and stand up slowly after you have been sitting or lying down. unusual urges. some people who take certain medicines to treat parkinson’s disease or rls, including pramipexole dihydrochloride tablets, have reported problems, such as gambling, compulsive eating, compulsive buying, and increased sex drive. if you or your family members notice that you are developing unusual urges or behaviors, talk to your doctor. hallucinations and other psychotic-like behavior (seeing visions, hearing sounds or feeling sensations that are not real, confusion, excessive suspicion, aggressive behavior, agitation, delusional beliefs and disorganized thinking). the chances of having hallucinations or other psychotic-like changes are higher in people taking pramipexole dihydrochloride tablets for parkinson’s disease who are elderly (age 65 or older). if you have hallucinations or other psychotic-like changes, talk with your doctor right away. uncontrolled sudden movements (dyskinesia). if you have new dyskinesia or your existing dyskinesia gets worse tell your doctor. posture changes. talk with your doctor if you have posture changes you cannot control. these may include your neck bending forward, bending forward at the waist, or tilting sideways when you sit, stand, or walk. withdrawal symptoms . pramipexole dihydrochloride tablets is a dopamine agonist medicine. dopamine agonist medicines, including pramipexole dihydrochloride tablets, can cause withdrawal symptoms as your dose is slowly lowered (tapered) or when treatment with pramipexole dihydrochloride tablets is stopped. tell your doctor right away if you get any of the following withdrawal symptoms: fever confusion severe muscle stiffness feeling like you do not care about things you usually care about (apathy) anxiety depression fatigue insomnia sweating pain after you have stopped taking pramipexole dihydrochloride tablets, your doctor may need to restart you at a low dose of pramipexole dihydrochloride tablets if you get severe withdrawal symptoms. the most common side effects in people taking pramipexole dihydrochloride tablets for restless legs syndrome are nausea and headache. the most common side effects in people taking pramipexole dihydrochloride tablets for parkinson’s disease are: nausea dizziness insomnia constipation muscle weakness abnormal dreams confusion memory problems (amnesia) urinating more often than normal these are not all the possible side effects of pramipexole dihydrochloride tablets. tell your doctor if you have any side effect that bothers you. call your doctor for medical advice about side effects. you may report side effects to fda at 1-800-fda-1088. how should i store pramipexole dihydrochloride tablets? store pramipexole dihydrochloride tablets at 20° to 25°c (68° to 77°f). keep pramipexole dihydrochloride tablets out of the light. keep pramipexole dihydrochloride tablets and all medicines out of the reach of children. general information about the safe and effective use of pramipexole dihydrochloride tablets. medicines are sometimes prescribed for purposes other than those listed in a patient information leaflet. do not use pramipexole dihydrochloride tablets for a condition for which it was not prescribed. do not give pramipexole dihydrochloride tablets to other people, even if they have the same symptoms that you have. they may harm them. this patient information leaflet summarizes the most important information about pramipexole dihydrochloride tablets. if you would like more information, talk with your doctor. you can ask your pharmacist or doctor for information about pramipexole dihydrochloride tablets that is written for healthcare professionals. for more information, call aurobindo pharma usa, inc. at 1-866-850-2876. what are the ingredients in pramipexole dihydrochloride tablets? active ingredient : pramipexole dihydrochloride inactive ingredients : colloidal silicon dioxide, corn starch, magnesium stearate, mannitol, and povidone this patient information has been approved by the u.s. food and drug administration. all brands listed are the trademarks of their respective owners and are not trademarks of aurobindo pharma limited. distributed by: aurobindo pharma usa, inc. 279 princeton-hightstown road east windsor, nj 08520 manufactured by: aurobindo pharma limited hyderabad-500 032, india revised: 07/2021