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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 PROTOPIC Cause Condition aggravated? 6 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 6 reports of Condition aggravated have been filed in association with PROTOPIC. This represents 3.9% of all adverse event reports for PROTOPIC.

6
Reports of Condition aggravated with PROTOPIC
3.9%
of all PROTOPIC reports
0
Deaths
0
Hospitalizations

How Dangerous Is Condition aggravated From PROTOPIC?

Of the 6 reports.

Is Condition aggravated Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for PROTOPIC. However, 6 reports have been filed with the FAERS database.

What Other Side Effects Does PROTOPIC Cause?

Off label use (83) Pruritus (14) Burning sensation (9) Drug ineffective (9) Hypersensitivity (7) Application site pain (6) Drug prescribing error (6) Skin burning sensation (6) Acne (5) Rash (5)

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 PROTOPIC Alternatives Have Lower Condition aggravated Risk?

PROTOPIC vs PROVENGE PROTOPIC vs PROVENTIL PROTOPIC vs PROVERA PROTOPIC vs PROZAC PROTOPIC vs PRUCALOPRIDE

Related Pages

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