Does DIMENHYDRINATE Cause Product prescribing error? 101 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 101 reports of Product prescribing error have been filed in association with DIMENHYDRINATE (Driminate). This represents 5.2% of all adverse event reports for DIMENHYDRINATE.
101
Reports of Product prescribing error with DIMENHYDRINATE
5.2%
of all DIMENHYDRINATE reports
0
Deaths
96
Hospitalizations
How Dangerous Is Product prescribing error From DIMENHYDRINATE?
Of the 101 reports, 96 (95.0%) required hospitalization.
Is Product prescribing error Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for DIMENHYDRINATE. However, 101 reports have been filed with the FAERS database.
What Other Side Effects Does DIMENHYDRINATE Cause?
Fatigue (542)
Nausea (522)
Vomiting (436)
Malaise (426)
Anxiety (371)
Dizziness (358)
Headache (311)
Cystitis (302)
Chest discomfort (299)
Pyrexia (295)
What Other Drugs Cause Product prescribing error?
SOMATROPIN (1,123)
SACUBITRIL\VALSARTAN (1,023)
SECUKINUMAB (821)
TOFACITINIB (805)
DUPILUMAB (725)
NIRMATRELVIR\RITONAVIR (611)
PREGABALIN (476)
METHOTREXATE (434)
TORSEMIDE (352)
METOPROLOL (325)
Which DIMENHYDRINATE Alternatives Have Lower Product prescribing error Risk?
DIMENHYDRINATE vs DIMETHICONE
DIMENHYDRINATE vs DIMETHICONE\LOPERAMIDE
DIMENHYDRINATE vs DIMETHINDENE
DIMENHYDRINATE vs DIMETHYL
DIMENHYDRINATE vs DIMETHYL SULFONE