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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 GAMMA ORYZANOL Cause Product use issue? 12 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 12 reports of Product use issue have been filed in association with GAMMA ORYZANOL. This represents 50.0% of all adverse event reports for GAMMA ORYZANOL.

12
Reports of Product use issue with GAMMA ORYZANOL
50.0%
of all GAMMA ORYZANOL reports
0
Deaths
12
Hospitalizations

How Dangerous Is Product use issue From GAMMA ORYZANOL?

Of the 12 reports, 12 (100.0%) required hospitalization.

Is Product use issue Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for GAMMA ORYZANOL. However, 12 reports have been filed with the FAERS database.

What Other Side Effects Does GAMMA ORYZANOL Cause?

Abnormal behaviour (12) Drug interaction (12) Mood altered (12) Prescribed overdose (12) Stubbornness (12) Thinking abnormal (12) Prescribed underdose (9) Incorrect route of product administration (7) Product use in unapproved indication (7) Rash (5)

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)

Related Pages

GAMMA ORYZANOL Full Profile All Product use issue Reports All Drugs Causing Product use issue GAMMA ORYZANOL Demographics