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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 DROSPIRENONE Cause Hypersensitivity? 10 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 10 reports of Hypersensitivity have been filed in association with DROSPIRENONE (Angeliq). This represents 0.3% of all adverse event reports for DROSPIRENONE.

10
Reports of Hypersensitivity with DROSPIRENONE
0.3%
of all DROSPIRENONE reports
0
Deaths
2
Hospitalizations

How Dangerous Is Hypersensitivity From DROSPIRENONE?

Of the 10 reports, 2 (20.0%) required hospitalization.

Is Hypersensitivity Listed in the Official Label?

Yes, Hypersensitivity is listed as a known adverse reaction in the official FDA drug label for DROSPIRENONE.

What Other Side Effects Does DROSPIRENONE Cause?

Intermenstrual bleeding (1,086) Amenorrhoea (603) Heavy menstrual bleeding (436) Dysmenorrhoea (240) Product use in unapproved indication (154) Intentional dose omission (123) Nausea (118) Headache (117) Menstruation irregular (117) Product dose omission issue (116)

What Other Drugs Cause Hypersensitivity?

ETANERCEPT (10,846) ADALIMUMAB (10,641) METHOTREXATE (9,799) TOCILIZUMAB (9,076) ABATACEPT (8,945) INFLIXIMAB (8,519) RITUXIMAB (8,408) ADAPALENE (8,356) LEFLUNOMIDE (7,926) CERTOLIZUMAB PEGOL (7,353)

Which DROSPIRENONE Alternatives Have Lower Hypersensitivity Risk?

DROSPIRENONE vs DROSPIRENONE\ESTETROL DROSPIRENONE vs DROSPIRENONE\ESTRADIOL DROSPIRENONE vs DROSPIRENONE\ETHINYL ESTRADIOL DROSPIRENONE vs DROSPIRENONE\ETHINYL ESTRADIOL\LEVOMEFOLATE DROSPIRENONE vs DROTAVERINE

Related Pages

DROSPIRENONE Full Profile All Hypersensitivity Reports All Drugs Causing Hypersensitivity DROSPIRENONE Demographics