Does BETAHISTINE Cause Product administration error? 6 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 6 reports of Product administration error have been filed in association with BETAHISTINE. This represents 0.9% of all adverse event reports for BETAHISTINE.
6
Reports of Product administration error with BETAHISTINE
0.9%
of all BETAHISTINE reports
0
Deaths
6
Hospitalizations
How Dangerous Is Product administration error From BETAHISTINE?
Of the 6 reports, 6 (100.0%) required hospitalization, and 1 (16.7%) were considered life-threatening.
Is Product administration error Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for BETAHISTINE. However, 6 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 Product administration error?
HYDROXYPROGESTERONE CAPROATE (972)
ACETAMINOPHEN (666)
CENEGERMIN-BKBJ (613)
LEUPROLIDE (595)
EVOLOCUMAB (565)
ADALIMUMAB (543)
METHYLPHENIDATE (414)
OLMESARTAN MEDOXOMIL (314)
ASPIRIN (241)
SECUKINUMAB (225)
Which BETAHISTINE Alternatives Have Lower Product administration error Risk?
BETAHISTINE vs BETAINE
BETAHISTINE vs BETAMETHASONE
BETAHISTINE vs BETAMETHASONE DIPROPIONATE
BETAHISTINE vs BETAMETHASONE DIPROPIONATE\BETAMETHASONE
BETAHISTINE vs BETAMETHASONE DIPROPIONATE\CALCIPOTRIENE