Does DROSPIRENONE\ETHINYL ESTRADIOL Cause Product administration error? 6 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 6 reports of Product administration error have been filed in association with DROSPIRENONE\ETHINYL ESTRADIOL. This represents 0.1% of all adverse event reports for DROSPIRENONE\ETHINYL ESTRADIOL.
6
Reports of Product administration error with DROSPIRENONE\ETHINYL ESTRADIOL
0.1%
of all DROSPIRENONE\ETHINYL ESTRADIOL reports
0
Deaths
0
Hospitalizations
How Dangerous Is Product administration error From DROSPIRENONE\ETHINYL ESTRADIOL?
Of the 6 reports.
Is Product administration error Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for DROSPIRENONE\ETHINYL ESTRADIOL. However, 6 reports have been filed with the FAERS database.
What Other Side Effects Does DROSPIRENONE\ETHINYL ESTRADIOL Cause?
Pulmonary embolism (1,295)
Pain (1,286)
Injury (1,266)
Deep vein thrombosis (1,139)
Emotional distress (742)
Anxiety (623)
Cerebrovascular accident (528)
General physical health deterioration (498)
Thrombosis (403)
Headache (393)
What Other Drugs Cause Product administration error?
HYDROXYPROGESTERONE CAPROATE (972)
ACETAMINOPHEN (666)
CENEGERMIN-BKBJ (613)
LEUPROLIDE (595)
EVOLOCUMAB (565)
ADALIMUMAB (543)
METHYLPHENIDATE (414)
OLMESARTAN MEDOXOMIL (314)
ASPIRIN (241)
SECUKINUMAB (225)
Which DROSPIRENONE\ETHINYL ESTRADIOL Alternatives Have Lower Product administration error Risk?
DROSPIRENONE\ETHINYL ESTRADIOL vs DROSPIRENONE\ETHINYL ESTRADIOL\LEVOMEFOLATE
DROSPIRENONE\ETHINYL ESTRADIOL vs DROTAVERINE
DROSPIRENONE\ETHINYL ESTRADIOL vs DROXIDOPA
DROSPIRENONE\ETHINYL ESTRADIOL vs DULAGLUTIDE
DROSPIRENONE\ETHINYL ESTRADIOL vs DULERA