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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 Cognitive disorder? 5 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 5 reports of Cognitive disorder have been filed in association with REBOXETINE. This represents 2.7% of all adverse event reports for REBOXETINE.

5
Reports of Cognitive disorder with REBOXETINE
2.7%
of all REBOXETINE reports
1
Deaths
2
Hospitalizations

How Dangerous Is Cognitive disorder From REBOXETINE?

Of the 5 reports, 1 (20.0%) resulted in death, 2 (40.0%) required hospitalization, and 1 (20.0%) were considered life-threatening.

Is Cognitive disorder Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for REBOXETINE. However, 5 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) Intentional overdose (16) Nausea (16) Drug ineffective (15) Drug interaction (15) Sleep disorder (15)

What Other Drugs Cause Cognitive disorder?

CARBIDOPA\LEVODOPA (1,449) DIMETHYL (1,405) NATALIZUMAB (1,309) LEVOTHYROXINE (1,189) FINASTERIDE (1,074) INTERFERON BETA-1A (1,014) MORPHINE (929) FINGOLIMOD (919) CARBAMAZEPINE (849) AMITRIPTYLINE (834)

Which REBOXETINE Alternatives Have Lower Cognitive disorder 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 Cognitive disorder Reports All Drugs Causing Cognitive disorder REBOXETINE Demographics