Does DROSPIRENONE Cause Intentional dose omission? 123 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 123 reports of Intentional dose omission have been filed in association with DROSPIRENONE (Angeliq). This represents 3.8% of all adverse event reports for DROSPIRENONE.
123
Reports of Intentional dose omission with DROSPIRENONE
3.8%
of all DROSPIRENONE reports
0
Deaths
0
Hospitalizations
How Dangerous Is Intentional dose omission From DROSPIRENONE?
Of the 123 reports.
Is Intentional dose omission Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for DROSPIRENONE. However, 123 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)
Nausea (118)
Headache (117)
Menstruation irregular (117)
Product dose omission issue (116)
Wrong technique in product usage process (95)
What Other Drugs Cause Intentional dose omission?
DUPILUMAB (2,269)
CERTOLIZUMAB PEGOL (1,253)
ADALIMUMAB (845)
TOFACITINIB (845)
INFLIXIMAB (815)
ABALOPARATIDE (623)
ETANERCEPT (615)
AMBRISENTAN (595)
SODIUM OXYBATE (580)
CALCIUM OXYBATE\MAGNESIUM OXYBATE\POTASSIUM OXYBATE\SODIUM OXYBATE (518)
Which DROSPIRENONE Alternatives Have Lower Intentional dose omission Risk?
DROSPIRENONE vs DROSPIRENONE\ESTETROL
DROSPIRENONE vs DROSPIRENONE\ESTRADIOL
DROSPIRENONE vs DROSPIRENONE\ETHINYL ESTRADIOL
DROSPIRENONE vs DROSPIRENONE\ETHINYL ESTRADIOL\LEVOMEFOLATE
DROSPIRENONE vs DROTAVERINE