Does DROSPIRENONE Cause Wrong technique in product usage process? 95 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 95 reports of Wrong technique in product usage process have been filed in association with DROSPIRENONE (Angeliq). This represents 2.9% of all adverse event reports for DROSPIRENONE.
95
Reports of Wrong technique in product usage process with DROSPIRENONE
2.9%
of all DROSPIRENONE reports
0
Deaths
0
Hospitalizations
How Dangerous Is Wrong technique in product usage process From DROSPIRENONE?
Of the 95 reports.
Is Wrong technique in product usage process Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for DROSPIRENONE. However, 95 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 Wrong technique in product usage process?
EVOLOCUMAB (21,664)
ALBUTEROL (17,114)
ADALIMUMAB (11,766)
PEGFILGRASTIM (10,217)
ETANERCEPT (9,835)
ERENUMAB-AOOE (9,359)
SACUBITRIL\VALSARTAN (8,022)
LEUPROLIDE (5,062)
FENTANYL (2,812)
SEMAGLUTIDE (2,538)
Which DROSPIRENONE Alternatives Have Lower Wrong technique in product usage process Risk?
DROSPIRENONE vs DROSPIRENONE\ESTETROL
DROSPIRENONE vs DROSPIRENONE\ESTRADIOL
DROSPIRENONE vs DROSPIRENONE\ETHINYL ESTRADIOL
DROSPIRENONE vs DROSPIRENONE\ETHINYL ESTRADIOL\LEVOMEFOLATE
DROSPIRENONE vs DROTAVERINE