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Important: This site presents data from the FDA Adverse Event Reporting System (FAERS). A report does not mean the drug caused the event. Full disclaimer.

Does BETAHISTINE Cause Wrong technique in product usage process? 12 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 12 reports of Wrong technique in product usage process have been filed in association with BETAHISTINE. This represents 1.8% of all adverse event reports for BETAHISTINE.

12
Reports of Wrong technique in product usage process with BETAHISTINE
1.8%
of all BETAHISTINE reports
0
Deaths
1
Hospitalizations

How Dangerous Is Wrong technique in product usage process From BETAHISTINE?

Of the 12 reports, 1 (8.3%) required hospitalization.

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 BETAHISTINE. However, 12 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 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 BETAHISTINE Alternatives Have Lower Wrong technique in product usage process Risk?

BETAHISTINE vs BETAINE BETAHISTINE vs BETAMETHASONE BETAHISTINE vs BETAMETHASONE DIPROPIONATE BETAHISTINE vs BETAMETHASONE DIPROPIONATE\BETAMETHASONE BETAHISTINE vs BETAMETHASONE DIPROPIONATE\CALCIPOTRIENE

Related Pages

BETAHISTINE Full Profile All Wrong technique in product usage process Reports All Drugs Causing Wrong technique in product usage process BETAHISTINE Demographics