Not FDA approved for treatment of bipolar depression or children < 7 years Contraindications Hypersensitivity Concomitant pimozide or thioridazine (within 5 weeks of administering fluoxetine) Breastfeeding Coadministration with MAOIs Coadministration may cause serotonin syndrome Coadministration of MAOIs with ...
has been released. Since uptake is an important mechanism for removing released neurotransmitters and terminating their actions on adjacent nerves, the reduced uptake caused by fluoxetine increases free serotonin that stimulates nerve cells in the brain. The FDA approved Fluoxetine in December 1987. What...
The FDA approved Fluoxetine in December 1987. What brand names are available for fluoxetine? Prozac, Sarafem, Prozac Weekly Is fluoxetine available as a generic drug? Yes Do I need a prescription for fluoxetine? Yes What are the side effects of fluoxetine? Fluoxetine, as with most antidepressants...
Our Prozac Side Effects Drug Center provides a comprehensive view of available drug information on the potential side effects when taking this medication. CALL YOUR DOCTOR FOR MEDICAL ADVICE ABOUT SIDE EFFECTS. YOU MAY REPORT SIDE EFFECTS TO THE FDA AT 1-800-FDA-1088. WARNING SUICIDAL THOUGHTS A...
CALL YOUR DOCTOR FOR MEDICAL ADVICE ABOUT SIDE EFFECTS. YOU MAY REPORT SIDE EFFECTS TO THE FDA AT 1-800-FDA-1088. WARNING SUICIDAL THOUGHTS AND BEHAVIORS Antidepressants increased the risk of suicidal thoughts and behavior in children, adolescents, and young adults in short-term studies. These ...
Note:Medication side effects may be underreported. If you are experiencing side effects that are not listed, submit a report to the FDA by followingthis guide. Medical Disclaimer Drug Status AvailabilityPrescription onlyRx Pregnancy & LactationRisk data available ...
CALL YOUR DOCTOR FOR MEDICAL ADVICE ABOUT SIDE EFFECTS. YOU MAY REPORT SIDE EFFECTS TO THE FDA AT 1-800-FDA-1088. WARNING SUICIDAL THOUGHTS AND BEHAVIORS Antidepressants increased the risk of suicidal thoughts and behavior in children, adolescents, and young adults in short-term studies. These ...
CALL YOUR DOCTOR FOR MEDICAL ADVICE ABOUT SIDE EFFECTS. YOU MAY REPORT SIDE EFFECTS TO THE FDA AT 1-800-FDA-1088. WARNING SUICIDAL THOUGHTS AND BEHAVIORS Antidepressants increased the risk of suicidal thoughts and behavior in children, adolescents, and young adults in short-term studies. These ...
CALL YOUR DOCTOR FOR MEDICAL ADVICE ABOUT SIDE EFFECTS. YOU MAY REPORT SIDE EFFECTS TO THE FDA AT 1-800-FDA-1088. WARNING SUICIDAL THOUGHTS AND BEHAVIORS Antidepressants increased the risk of suicidal thoughts and behavior in children, adolescents, and young adults in short-term studies. These ...