Does DROSPIRENONE Cause Product dose omission in error? 10 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 10 reports of Product dose omission in error have been filed in association with DROSPIRENONE (Angeliq). This represents 0.3% of all adverse event reports for DROSPIRENONE.
10
Reports of Product dose omission in error with DROSPIRENONE
0.3%
of all DROSPIRENONE reports
0
Deaths
0
Hospitalizations
How Dangerous Is Product dose omission in error From DROSPIRENONE?
Of the 10 reports.
Is Product dose omission in error Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for DROSPIRENONE. However, 10 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 Product dose omission in error?
DUPILUMAB (7,586)
TOFACITINIB (2,461)
LENALIDOMIDE (618)
PALBOCICLIB (592)
DIROXIMEL (481)
ABALOPARATIDE (457)
NIRAPARIB (428)
RUXOLITINIB (425)
TERIFLUNOMIDE (371)
DIMETHYL (308)
Which DROSPIRENONE Alternatives Have Lower Product dose omission in error Risk?
DROSPIRENONE vs DROSPIRENONE\ESTETROL
DROSPIRENONE vs DROSPIRENONE\ESTRADIOL
DROSPIRENONE vs DROSPIRENONE\ETHINYL ESTRADIOL
DROSPIRENONE vs DROSPIRENONE\ETHINYL ESTRADIOL\LEVOMEFOLATE
DROSPIRENONE vs DROTAVERINE