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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 BETAINE Cause Off label use? 138 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 138 reports of Off label use have been filed in association with BETAINE (Stomach Enzyme Formula). This represents 16.3% of all adverse event reports for BETAINE.

138
Reports of Off label use with BETAINE
16.3%
of all BETAINE reports
9
Deaths
65
Hospitalizations

How Dangerous Is Off label use From BETAINE?

Of the 138 reports, 9 (6.5%) resulted in death, 65 (47.1%) required hospitalization, and 3 (2.2%) were considered life-threatening.

Is Off label use Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for BETAINE. However, 138 reports have been filed with the FAERS database.

What Other Side Effects Does BETAINE Cause?

Overdose (83) Vomiting (67) Product dose omission (55) Diarrhoea (53) Product use issue (42) Seizure (41) Product dose omission issue (36) Inappropriate schedule of product administration (35) Nausea (34) Pneumonia (32)

What Other Drugs Cause Off label use?

RITUXIMAB (39,751) INFLIXIMAB (34,801) DENOSUMAB (34,612) METHOTREXATE (24,020) VEDOLIZUMAB (21,017) ETANERCEPT (20,178) TOCILIZUMAB (18,256) PREDNISONE (17,867) LENALIDOMIDE (17,017) ADALIMUMAB (16,417)

Which BETAINE Alternatives Have Lower Off label use Risk?

BETAINE vs BETAMETHASONE BETAINE vs BETAMETHASONE DIPROPIONATE BETAINE vs BETAMETHASONE DIPROPIONATE\BETAMETHASONE BETAINE vs BETAMETHASONE DIPROPIONATE\CALCIPOTRIENE BETAINE vs BETAMETHASONE DIPROPIONATE\CALCIPOTRIENE HYDRATE

Related Pages

BETAINE Full Profile All Off label use Reports All Drugs Causing Off label use BETAINE Demographics