Does TOPIRAMATE Cause Wrong technique in product usage process? 108 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 108 reports of Wrong technique in product usage process have been filed in association with TOPIRAMATE (Topiramate). This represents 0.4% of all adverse event reports for TOPIRAMATE.
108
Reports of Wrong technique in product usage process with TOPIRAMATE
0.4%
of all TOPIRAMATE reports
1
Deaths
16
Hospitalizations
How Dangerous Is Wrong technique in product usage process From TOPIRAMATE?
Of the 108 reports, 1 (0.9%) resulted in death, 16 (14.8%) required hospitalization, and 1 (0.9%) were considered life-threatening.
Is Wrong technique in product usage process Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for TOPIRAMATE. However, 108 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 Wrong technique in product usage process?
EVOLOCUMAB (21,664)
ALBUTEROL (17,114)
ADALIMUMAB (11,766)
PEGFILGRASTIM (10,217)
ETANERCEPT (9,835)
ERENUMAB-AOOE (9,359)
SACUBITRIL\VALSARTAN (8,022)
LEUPROLIDE (5,062)
FENTANYL (2,812)
SEMAGLUTIDE (2,538)
Which TOPIRAMATE Alternatives Have Lower Wrong technique in product usage process Risk?
TOPIRAMATE vs TOPOTECAN
TOPIRAMATE vs TOPOTECAN\TOPOTECAN
TOPIRAMATE vs TOPROL
TOPIRAMATE vs TOREMIFENE
TOPIRAMATE vs TORIPALIMAB