Does BETAHISTINE Cause Incorrect product administration duration? 8 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 8 reports of Incorrect product administration duration have been filed in association with BETAHISTINE. This represents 1.2% of all adverse event reports for BETAHISTINE.
8
Reports of Incorrect product administration duration with BETAHISTINE
1.2%
of all BETAHISTINE reports
0
Deaths
6
Hospitalizations
How Dangerous Is Incorrect product administration duration From BETAHISTINE?
Of the 8 reports, 6 (75.0%) required hospitalization, and 1 (12.5%) 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 BETAHISTINE. However, 8 reports have been filed with the FAERS database.
What Other Side Effects Does BETAHISTINE Cause?
Dizziness (121)
Hypotension (102)
Fall (100)
Nausea (96)
Vomiting (81)
Drug ineffective (80)
Hypersensitivity (67)
Constipation (60)
Hyponatraemia (59)
Vertigo (56)
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 BETAHISTINE Alternatives Have Lower Incorrect product administration duration Risk?
BETAHISTINE vs BETAINE
BETAHISTINE vs BETAMETHASONE
BETAHISTINE vs BETAMETHASONE DIPROPIONATE
BETAHISTINE vs BETAMETHASONE DIPROPIONATE\BETAMETHASONE
BETAHISTINE vs BETAMETHASONE DIPROPIONATE\CALCIPOTRIENE