Does DROSPIRENONE Cause Condition aggravated? 51 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 51 reports of Condition aggravated have been filed in association with DROSPIRENONE (Angeliq). This represents 1.6% of all adverse event reports for DROSPIRENONE.
51
Reports of Condition aggravated with DROSPIRENONE
1.6%
of all DROSPIRENONE reports
2
Deaths
5
Hospitalizations
How Dangerous Is Condition aggravated From DROSPIRENONE?
Of the 51 reports, 2 (3.9%) resulted in death, 5 (9.8%) required hospitalization, and 4 (7.8%) 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 DROSPIRENONE. However, 51 reports have been filed with the FAERS database.
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 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 DROSPIRENONE Alternatives Have Lower Condition aggravated Risk?
DROSPIRENONE vs DROSPIRENONE\ESTETROL
DROSPIRENONE vs DROSPIRENONE\ESTRADIOL
DROSPIRENONE vs DROSPIRENONE\ETHINYL ESTRADIOL
DROSPIRENONE vs DROSPIRENONE\ETHINYL ESTRADIOL\LEVOMEFOLATE
DROSPIRENONE vs DROTAVERINE