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When adjunctive abilify is administered to patients with major depressive disorder, abilify should be administered without dosage adjustment as specified in sections above.

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Before prescribing the new pill and tracking system, doctors should ensure that their patients are capable of and dedicated to using the system, says the FDA. The drug Abilify (with or without the digital sensor can cause side effects including nausea, vomiting, constipation, anxiety, headache and uncontrollable movements. The MyCite stick-on patch may cause skin irritation in some people.

Cerebrovascular Adverse Reactions in Elderly Patients with Dementia-Related Psychosis: Increased incidence of cerebrovascular adverse reactions (e.g. stroke, transient ischemic attack, including fatalities). Neuroleptic Malignant Syndrome: Manage with immediate discontinuation and close monitoring. Tardive Dyskinesia: Discontinue if clinically appropriate. Metabolic Changes: Atypical antipsychotic drugs have been associated with metabolic changes that include hyperglycemia/diabetes mellitus, dyslipidemia, and body weight gain. Hyperglycemia/Diabetes Mellitus: Monitor glucose regularly in patients with and at risk for diabetes. Dyslipidemia: Undesirable alterations in lipid levels have been observed in patients treated with atypical antipsychotics. Weight Gain: Weight gain has been observed with atypical antipsychotic use. Monitor weight. Pathological Gambling and Other Compulsive Behaviors: Consider dose reduction or discontinuation. Falls: Antipsychotics may cause somnolence, postural hypotension, motor and sensory instability, which may lead zolpidem. to falls. Orthostatic Hypotension: Monitor heart rate and blood pressure and warn patients with known cardiovascular or cerebrovascular disease, and risk of dehydration or syncope. Leukopenia, Neutropenia, and Agranulocytosis: have been reported with antipsychotics including ABILIFY. Patients with a history of a clinically significant low white blood cell count (WBC or a drug-induced leukopenia/neutropenia should have their complete blood count (CBC monitored frequently during the first few months of therapy and discontinuation of ABILIFY should be considered at the first sign of a clinically significant decline in WBC in the absence of other causative factors. Seizures/Convulsions: Use cautiously in patients with a history of seizures or with conditions that lower the seizure threshold. Potential for Cognitive and Motor Impairment: Use caution when operating machinery. Suicide: The possibility of a suicide attempt is inherent in schizophrenia and bipolar disorder. Closely supervise high-risk patients.

If you have an allergy to any one of the ingredients present in Abilify, including aripiprazole, you should not take the drug. Abilify should not be used for treating patients with dementia-related psychosis or suicidal thoughts, as it can lead to an increased risk of death in these patients.

Before taking Abilify, inform your doctor or healthcare provider of any medical conditions you currently have or have had in the past. This includes diabetes, high blood sugar, seizures, low blood pressure, high blood pressure, a low count of white blood cells, phenylketonuria, and stroke or heart problems. Make sure your doctor knows about any the medications you currently take, including herbal supplements, prescription and over-the-counter drugs, and vitamins. Never stop taking Abilify or any other prescription drug without first seeking medical advice from your healthcare provider.

Abilify MyCite is approved for the treatment of schizophrenia and bipolar I disorder, and as an add-on treatment for depression in adults.

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