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The Oleptro brand name has been discontinued in the U.S. for reasons unrelated to safety or efficacy. Other brand names or generic alternatives may be available. If you’re currently taking this medication, talk to your healthcare provider about safe options for transitioning to a different treatment.

Overview

Oleptro was a prescription drug approved by the U.S. Food and Drug Administration (FDA) to treat major depressive disorder in adults. Oleptro was also referred to by its drug name, trazodone. 

Oleptro was an atypical antidepressant. It was known as a serotonin modulator. Oleptro was believed to work by changing the balance of neurotransmitters in the brain.

How was it taken?

Oleptro was generally taken once daily. Oleptro came in tablet form.

Side effects

The FDA-approved label for Oleptro listed common side effects including drowsiness, dizziness, headache, blurred vision, dry mouth, constipation, vomiting, and changes in sexual interest or ability. 

Rare but serious side effects listed for Oleptro included worsening of depression symptoms, increased suicide risk, and serotonin syndrome, which may be life-threatening. 

For more details about this treatment, visit:

Trazodone — DailyMed

 

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