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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 RETINOL Cause Condition aggravated? 31 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 31 reports of Condition aggravated have been filed in association with RETINOL (HYDRASPHERE PLUS). This represents 10.5% of all adverse event reports for RETINOL.

31
Reports of Condition aggravated with RETINOL
10.5%
of all RETINOL reports
29
Deaths
29
Hospitalizations

How Dangerous Is Condition aggravated From RETINOL?

Of the 31 reports, 29 (93.5%) resulted in death, 29 (93.5%) required hospitalization, and 23 (74.2%) were considered life-threatening.

Is Condition aggravated Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for RETINOL. However, 31 reports have been filed with the FAERS database.

What Other Side Effects Does RETINOL Cause?

Gastrooesophageal reflux disease (113) Somnolence (86) Coma (85) Pneumonia aspiration (85) Off label use (82) Drug ineffective (64) Infusion related reaction (49) Type 2 diabetes mellitus (49) Confusional state (45) Pain (44)

What Other Drugs Cause Condition aggravated?

TOFACITINIB (16,925) INFLIXIMAB (16,616) DUPILUMAB (16,459) ETANERCEPT (15,897) METHOTREXATE (14,938) ADALIMUMAB (13,527) PREDNISONE (10,751) INFLIXIMAB-DYYB (10,275) HYDROXYCHLOROQUINE (8,848) RITUXIMAB (8,627)

Which RETINOL Alternatives Have Lower Condition aggravated Risk?

RETINOL vs REVATIO RETINOL vs REVEFENACIN RETINOL vs REVLIMID RETINOL vs REVOLADE RETINOL vs REVUMENIB

Related Pages

RETINOL Full Profile All Condition aggravated Reports All Drugs Causing Condition aggravated RETINOL Demographics