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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 HERBALS\KARAYA GUM Cause Incorrect product administration duration? 9 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 9 reports of Incorrect product administration duration have been filed in association with HERBALS\KARAYA GUM. This represents 17.3% of all adverse event reports for HERBALS\KARAYA GUM.

9
Reports of Incorrect product administration duration with HERBALS\KARAYA GUM
17.3%
of all HERBALS\KARAYA GUM reports
0
Deaths
0
Hospitalizations

How Dangerous Is Incorrect product administration duration From HERBALS\KARAYA GUM?

Of the 9 reports.

Is Incorrect product administration duration Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for HERBALS\KARAYA GUM. However, 9 reports have been filed with the FAERS database.

What Other Side Effects Does HERBALS\KARAYA GUM Cause?

Hypertension (12) Weight increased (12) Off label use (9) Wrong technique in product usage process (9) Cholestasis (8) Food allergy (8) Thyroid gland injury (8) Acute kidney injury (6) Oliguria (5) Respiratory distress (5)

What Other Drugs Cause Incorrect product administration duration?

ETONOGESTREL (3,974) POLYETHYLENE GLYCOL 3350 (2,129) NIRMATRELVIR\RITONAVIR (744) DOCOSANOL (634) LANSOPRAZOLE (564) LOPERAMIDE (543) NAPROXEN (499) INSULIN LISPRO (479) DICLOFENAC (362) OMEPRAZOLE (302)

Related Pages

HERBALS\KARAYA GUM Full Profile All Incorrect product administration duration Reports All Drugs Causing Incorrect product administration duration HERBALS\KARAYA GUM Demographics