Does BETAINE Cause Product use issue? 42 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 42 reports of Product use issue have been filed in association with BETAINE (Stomach Enzyme Formula). This represents 5.0% of all adverse event reports for BETAINE.
42
Reports of Product use issue with BETAINE
5.0%
of all BETAINE reports
5
Deaths
12
Hospitalizations
How Dangerous Is Product use issue From BETAINE?
Of the 42 reports, 5 (11.9%) resulted in death, 12 (28.6%) required hospitalization, and 4 (9.5%) were considered life-threatening.
Is Product use issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for BETAINE. However, 42 reports have been filed with the FAERS database.
What Other Side Effects Does BETAINE Cause?
Off label use (138)
Overdose (83)
Vomiting (67)
Product dose omission (55)
Diarrhoea (53)
Seizure (41)
Product dose omission issue (36)
Inappropriate schedule of product administration (35)
Nausea (34)
Pneumonia (32)
What Other Drugs Cause Product use issue?
INFLIXIMAB (12,752)
DUPILUMAB (10,575)
POLYETHYLENE GLYCOL 3350 (9,432)
METHOTREXATE (8,185)
DICLOFENAC (8,009)
RITUXIMAB (6,948)
ADALIMUMAB (6,379)
ETANERCEPT (6,062)
TOCILIZUMAB (5,944)
ABATACEPT (5,915)
Which BETAINE Alternatives Have Lower Product use issue Risk?
BETAINE vs BETAMETHASONE
BETAINE vs BETAMETHASONE DIPROPIONATE
BETAINE vs BETAMETHASONE DIPROPIONATE\BETAMETHASONE
BETAINE vs BETAMETHASONE DIPROPIONATE\CALCIPOTRIENE
BETAINE vs BETAMETHASONE DIPROPIONATE\CALCIPOTRIENE HYDRATE