Does ETHINYL ESTRADIOL\NORGESTIMATE Cause Product dose omission? 152 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 152 reports of Product dose omission have been filed in association with ETHINYL ESTRADIOL\NORGESTIMATE. This represents 3.1% of all adverse event reports for ETHINYL ESTRADIOL\NORGESTIMATE.
152
Reports of Product dose omission with ETHINYL ESTRADIOL\NORGESTIMATE
3.1%
of all ETHINYL ESTRADIOL\NORGESTIMATE reports
0
Deaths
1
Hospitalizations
How Dangerous Is Product dose omission From ETHINYL ESTRADIOL\NORGESTIMATE?
Of the 152 reports, 1 (0.7%) required hospitalization.
Is Product dose omission Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ETHINYL ESTRADIOL\NORGESTIMATE. However, 152 reports have been filed with the FAERS database.
What Other Side Effects Does ETHINYL ESTRADIOL\NORGESTIMATE Cause?
Drug dose omission (950)
Inappropriate schedule of drug administration (724)
Nausea (315)
Vaginal haemorrhage (285)
Metrorrhagia (264)
Product use issue (257)
Anxiety (225)
Drug ineffective (225)
Headache (202)
Pregnancy on oral contraceptive (197)
What Other Drugs Cause Product dose omission?
APREMILAST (4,567)
DUPILUMAB (2,729)
ALBUTEROL (1,742)
USTEKINUMAB (1,653)
INSULIN GLARGINE (1,500)
ETANERCEPT (1,400)
LENALIDOMIDE (1,400)
RUXOLITINIB (1,376)
ALIROCUMAB (1,354)
DIMETHYL (1,248)
Which ETHINYL ESTRADIOL\NORGESTIMATE Alternatives Have Lower Product dose omission Risk?
ETHINYL ESTRADIOL\NORGESTIMATE vs ETHINYL ESTRADIOL\NORGESTREL
ETHINYL ESTRADIOL\NORGESTIMATE vs ETHINYL ESTRADIOL\SEGESTERONE
ETHINYL ESTRADIOL\NORGESTIMATE vs ETHIODIZED OIL
ETHINYL ESTRADIOL\NORGESTIMATE vs ETHIONAMIDE
ETHINYL ESTRADIOL\NORGESTIMATE vs ETHOSUXIMIDE