Does NORGESTREL Cause Product dose omission issue? 26 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 26 reports of Product dose omission issue have been filed in association with NORGESTREL (Opill). This represents 6.4% of all adverse event reports for NORGESTREL.
26
Reports of Product dose omission issue with NORGESTREL
6.4%
of all NORGESTREL reports
0
Deaths
0
Hospitalizations
How Dangerous Is Product dose omission issue From NORGESTREL?
Of the 26 reports.
Is Product dose omission issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for NORGESTREL. However, 26 reports have been filed with the FAERS database.
What Other Side Effects Does NORGESTREL Cause?
Heavy menstrual bleeding (85)
Intermenstrual bleeding (57)
Polymenorrhoea (53)
Nausea (32)
Headache (28)
Pregnancy on oral contraceptive (26)
Dysmenorrhoea (21)
Product use in unapproved indication (18)
Vaginal haemorrhage (18)
Depression (17)
What Other Drugs Cause Product dose omission issue?
DUPILUMAB (18,189)
USTEKINUMAB (9,405)
GUSELKUMAB (9,267)
LENALIDOMIDE (8,145)
MEPOLIZUMAB (5,873)
TOFACITINIB (5,646)
VOXELOTOR (5,122)
BELIMUMAB (4,671)
SECUKINUMAB (4,572)
APREMILAST (4,460)
Which NORGESTREL Alternatives Have Lower Product dose omission issue Risk?
NORGESTREL vs NORTRIPTYLINE
NORGESTREL vs NORVASC
NORGESTREL vs NORVIR
NORGESTREL vs NOSCAPINE
NORGESTREL vs NOVOLOG