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The most common side-effects are feeling tired, cold hands and feet, disturbed sleep, and stomach upset. Artane. informational and educational purposes only. Find patient medical information for Aricept Oral on WebMD including its uses, side effects and safety, interactions, pictures, warnings and user ratings.

and formulary information changes. Controlled studies in pregnant women show no evidence of fetal risk.Non-ergot dopamine D2 receptor agonist; strong affinity for D2 and D3 receptors; binding to these receptors increases dopamine activity on nerves of striatum and substantia nigraPeak plasma time: Immediate release, 2 hr; extended release, 6 hrAdding plans allows you to compare formulary status to other drugs in the same class.To view formulary information first create a list of plans. Immediate-release: 0.125 mg PO q8hr initially; gradually titrated upward at weekly intervals to target range of 1.5-4.5 mg/day PO divided q8hrExtended-release: 0.375 mg/day PO initially; if necessary, may be increased every 5-7 days, first to 0.75 mg/day and then by increments of 0.75 mg/day; not to exceed 4.5 mg/day0.125 mg/day PO 2-3 hr before bedtime initially; may be increased every 4-7 days up to 0.5 mg/day (every 14 days if CrCl 20-60 mL/min)Hepatic impairmet: No dosage adjustments provided in the manufacturer's labeling; adjustment not expected; undergoes minimal hepatic metabolismMay switch overnight from immediate-release to extended-release tablets at same daily dose; dose adjustments may be required for some patientsExtended-release: Swallow whole; do not chew, crush, or divideDiscontinuing immediate- or extended-release: Taper off at a rate of 0.75 mg/day until the daily dose has been reduced to 0.75 mg; thereafter, the dose may be reduced by 0.375 mg/dayTreatment of Tourette syndrome in pediatric patientsSome variations between early Parkinson, advanced Parkinson, and restless legs syndromeIncidence of some adverse drug reactions (eg, dizziness, accidental injury) >10% but comparable to placeboNeurologic: Abnormal behavior, abnormal dreams, compulsive shopping, fatigue, hallucinations (all kinds), headache, pathologic gamblingCardiovascular: Hypotension (including syncope and postural hypotension)Metabolic: Increased eating (including binge eating, compulsive eating, and hyperphagia), weight gain, SIADHDermatologic: Skin reactions, including rythema, rash, pruritus, urticariaGenitourinary: Libido disorders (including increased or decreased libido and hypersexuality)May cause sudden daytime "sleep attacks;" inquire about factors that may increase risk of falling asleep, including sleep disorders or taking sedating medications; caution patients about performing tasks requiring mental alertness; discontinue if there is evidence of sleep attacks; if decision is made to continue therapy, advice patient not to perform dangerous activities requiring mental alertnessOrthostatic hypotension may occur, particularly during dose escalation; monitor closely Parkinson patients being treated with dopaminergic agonists, especially during dose escalationIn early Parkinson, dosages higher than 1.5 mg q8hr provided no additional benefit but increased adverse eventsUse with caution in renal impairment; dose adjustment may be necessary; do not administer extended release tablets to patients with CrCl<30 mL/min or ESRD requiring hemodialysisAugmentation or rebound of restless legs syndrome (RLS) may occur with therapy in RLS patientsSwallow whole; do not chew, crush, or divide extended release tabletsEvents reported with dopaminergic therapy include hyperpyrexia and confusionFibrotic complications reported with use; monitor closely for signs and symptoms of fibrosis; discontinuation of therapy may resolve complications but not in all casesRsk of melanoma increases in Parkinson disease patients; monitor closely and perform periodic skin examinationPathologic degenerative changes observed in retinas of albino rats during studies; significance in humans unclearMay cause or exacerbate dyskinesia; use with caution in patients with preexisting dyskinesiasSymptoms resembling neuroleptic malignant syndrome, including elevated temperature, muscular rigidity, altered consciousness, and autonomic instability reported with rapid dose reduction, discontinuation, or changes in therapy; taper dose to decrease risk of hyperpyrexia and confusionGradual discontinuance required over period of 1 week or longer; symptoms resembling neuroleptic malignant syndrome may occur on abrupt withdrawalRisk of new-onset heart failure undergoing FDA evaluation (FDA safety announcement 9/19/2012)There are no adequate data on the developmental risk associated with therapy in pregnant women; no adverse developmental effects reported in animal studies in which pramipexole was administered to rabbits during pregnancy; effects on embryofetal development could not be adequately assessed in pregnant rats; however, postnatal growth was inhibited at clinically relevant exposuresIn the U.S. general population, the estimated background risk of major birth defects and of miscarriage in clinically recognized pregnancies is 2-4% and 15-20%, respectively; background risk of major birth defects and miscarriage for the indicated population is unknownLactation: Not known if drug secreted in breast milk; may inhibit milk production; discontinue drug, or do not nurseA: Generally acceptable.

monitor for orthostatic hypotension, EPS. PREPARE: Direct: Dilute 25 mg with 24 mL of NS to yield 1 mg/mL. Properly discard this product when it is expired or no longer needed. If you notice other effects not listed above, contact your doctor or pharmacist.Call your doctor for medical advice about side effects. Before using donepezil, tell your doctor or pharmacist of all the drugs you take and if you have any of the following conditions: certain Older adults may be more sensitive to the side effects of this drug, especially QT prolongation (see above).Some products that may interact with this drug include: Check all prescription and nonprescription medicine labels carefully since many medications contain pain relievers/fever reducers (NSAIDs such as If someone has overdosed and has serious symptoms such as passing out or If you miss a dose, skip the missed dose. Your list will be saved and can be edited at any time.The above information is provided for general 2002 Continuous: Give slowly at a rate not to exceed 1 mg/min. Do not stop taking it unless your doctor instructs you to do so. News

Medscape - Generalized anxiety disorder-specific dosing for BuSpar (buspirone), frequency-based adverse effects, comprehensive interactions, contraindications, pregnancy & …

Medscape - Parkinson disease-specific dosing for Mirapex, Mirapex ER (pramipexole), frequency-based adverse effects, comprehensive interactions, contraindications, pregnancy & … Consult your Are you planning to see a doctor about switching your medication?Are you planning to see a doctor about switching your medication?Selected from data included with permission and copyrighted by First Databank, Inc. Individual plans may vary

You may need to start at a lower dose to decrease the risk of side effects.Use this medication regularly in order to get the most benefit from it.

Trihexyphenidyl (THP) and other antiparkinsonian drugs are known to be substances of abuse.

2002 If you are unsure why you are taking it, speak with your doctor.

Intravenous. dermatologic exams important.

Propranolol is prescribed to treat a number of different conditions. Do not double the dose to catch up.Store at room temperature away from light and moisture. It may take a several weeks before you get the full benefit of this drug.Tell your doctor right away if any of these serious side effects occur: trouble urinating, severe Get medical help right away if you have any very serious side effects, including: slow/fast/irregular heartbeat, severe dizziness, This is not a complete list of possible side effects.