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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 CALCIPOTRIENE Cause Condition aggravated? 28 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 28 reports of Condition aggravated have been filed in association with CALCIPOTRIENE (SORILUX). This represents 2.1% of all adverse event reports for CALCIPOTRIENE.

28
Reports of Condition aggravated with CALCIPOTRIENE
2.1%
of all CALCIPOTRIENE reports
0
Deaths
1
Hospitalizations

How Dangerous Is Condition aggravated From CALCIPOTRIENE?

Of the 28 reports, 1 (3.6%) required hospitalization.

Is Condition aggravated Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for CALCIPOTRIENE. However, 28 reports have been filed with the FAERS database.

What Other Side Effects Does CALCIPOTRIENE Cause?

Drug ineffective (663) Psoriasis (342) Product use in unapproved indication (147) Therapeutic product effect incomplete (123) Pruritus (108) Treatment failure (102) Skin exfoliation (97) Arthralgia (81) Erythema (79) Rash (75)

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 CALCIPOTRIENE Alternatives Have Lower Condition aggravated Risk?

CALCIPOTRIENE vs CALCITONIN CALCIPOTRIENE vs CALCITONIN SALMON CALCIPOTRIENE vs CALCITRIOL CALCIPOTRIENE vs CALCITRIOL\CALCIUM\ZINC CALCIPOTRIENE vs CALCIUM

Related Pages

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