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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 GESTODENE Cause Condition aggravated? 21 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 21 reports of Condition aggravated have been filed in association with GESTODENE. This represents 63.6% of all adverse event reports for GESTODENE.

21
Reports of Condition aggravated with GESTODENE
63.6%
of all GESTODENE reports
0
Deaths
1
Hospitalizations

How Dangerous Is Condition aggravated From GESTODENE?

Of the 21 reports, 1 (4.8%) required hospitalization, and 1 (4.8%) 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 GESTODENE. However, 21 reports have been filed with the FAERS database.

What Other Side Effects Does GESTODENE Cause?

Drug interaction (23) Generalised tonic-clonic seizure (19) Drug level decreased (18) Drug ineffective (15) Blood oestrogen increased (11) Cerebral venous thrombosis (5) Off label use (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)

Related Pages

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