Does TOPIRAMATE Cause Incorrect product administration duration? 65 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 65 reports of Incorrect product administration duration have been filed in association with TOPIRAMATE (Topiramate). This represents 0.2% of all adverse event reports for TOPIRAMATE.
65
Reports of Incorrect product administration duration with TOPIRAMATE
0.2%
of all TOPIRAMATE reports
59
Deaths
59
Hospitalizations
How Dangerous Is Incorrect product administration duration From TOPIRAMATE?
Of the 65 reports, 59 (90.8%) resulted in death, 59 (90.8%) required hospitalization, and 58 (89.2%) were considered life-threatening.
Is Incorrect product administration duration Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for TOPIRAMATE. However, 65 reports have been filed with the FAERS database.
What Other Side Effects Does TOPIRAMATE Cause?
Drug ineffective (5,553)
Off label use (4,248)
Product use in unapproved indication (2,173)
Headache (1,997)
Drug intolerance (1,820)
Migraine (1,796)
Nausea (1,691)
Seizure (1,535)
Paraesthesia (1,506)
Dizziness (1,466)
What Other Drugs Cause Incorrect product administration duration?
ETONOGESTREL (3,974)
POLYETHYLENE GLYCOL 3350 (2,129)
NIRMATRELVIR\RITONAVIR (744)
DOCOSANOL (634)
LANSOPRAZOLE (564)
LOPERAMIDE (543)
NAPROXEN (499)
INSULIN LISPRO (479)
DICLOFENAC (362)
OMEPRAZOLE (302)
Which TOPIRAMATE Alternatives Have Lower Incorrect product administration duration Risk?
TOPIRAMATE vs TOPOTECAN
TOPIRAMATE vs TOPOTECAN\TOPOTECAN
TOPIRAMATE vs TOPROL
TOPIRAMATE vs TOREMIFENE
TOPIRAMATE vs TORIPALIMAB