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Important: This site presents data from the FDA Adverse Event Reporting System (FAERS). A report does not mean the drug caused the event. Full disclaimer.

Does REBOXETINE Cause Intentional overdose? 16 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 16 reports of Intentional overdose have been filed in association with REBOXETINE. This represents 8.7% of all adverse event reports for REBOXETINE.

16
Reports of Intentional overdose with REBOXETINE
8.7%
of all REBOXETINE reports
2
Deaths
10
Hospitalizations

How Dangerous Is Intentional overdose From REBOXETINE?

Of the 16 reports, 2 (12.5%) resulted in death, 10 (62.5%) required hospitalization, and 1 (6.3%) were considered life-threatening.

Is Intentional overdose Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for REBOXETINE. However, 16 reports have been filed with the FAERS database.

What Other Side Effects Does REBOXETINE Cause?

Hyperhidrosis (21) Off label use (20) Weight increased (18) Tachycardia (17) Confusional state (16) Nausea (16) Drug ineffective (15) Drug interaction (15) Sleep disorder (15) Alanine aminotransferase increased (14)

What Other Drugs Cause Intentional overdose?

ACETAMINOPHEN (6,869) QUETIAPINE (3,926) AMLODIPINE (3,427) PROMETHAZINE (3,193) IBUPROFEN (3,185) SERTRALINE (2,540) ALPRAZOLAM (2,389) DIAZEPAM (2,260) VENLAFAXINE (2,187) BUPROPION (2,103)

Which REBOXETINE Alternatives Have Lower Intentional overdose Risk?

REBOXETINE vs RECLAST REBOXETINE vs RECOMBINANT VARICELLA ZOSTER VIRUS GLYCOPROTEIN E REBOXETINE vs REGADENOSON REBOXETINE vs REGORAFENIB REBOXETINE vs REGORAFENIB\REGORAFENIB

Related Pages

REBOXETINE Full Profile All Intentional overdose Reports All Drugs Causing Intentional overdose REBOXETINE Demographics