Does NORETHINDRONE Cause Intentional product use issue? 5 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 5 reports of Intentional product use issue have been filed in association with NORETHINDRONE (ERRIN). This represents 0.3% of all adverse event reports for NORETHINDRONE.
5
Reports of Intentional product use issue with NORETHINDRONE
0.3%
of all NORETHINDRONE reports
2
Deaths
2
Hospitalizations
How Dangerous Is Intentional product use issue From NORETHINDRONE?
Of the 5 reports, 2 (40.0%) resulted in death, 2 (40.0%) required hospitalization, and 2 (40.0%) were considered life-threatening.
Is Intentional product use issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for NORETHINDRONE. However, 5 reports have been filed with the FAERS database.
What Other Side Effects Does NORETHINDRONE Cause?
Hot flush (195)
Nausea (155)
Vaginal haemorrhage (153)
Headache (141)
Off label use (131)
Drug ineffective (121)
Pelvic pain (113)
Fatigue (110)
Abdominal pain (100)
Menorrhagia (98)
What Other Drugs Cause Intentional product use issue?
INFLIXIMAB (11,028)
RITUXIMAB (9,602)
INFLIXIMAB-DYYB (7,549)
TOCILIZUMAB (5,078)
METHOTREXATE (4,087)
PREDNISONE (3,961)
ABATACEPT (3,693)
ADALIMUMAB (3,557)
NIVOLUMAB (3,297)
LEFLUNOMIDE (3,280)
Which NORETHINDRONE Alternatives Have Lower Intentional product use issue Risk?
NORETHINDRONE vs NORFLOXACIN
NORETHINDRONE vs NORGESTREL
NORETHINDRONE vs NORTRIPTYLINE
NORETHINDRONE vs NORVASC
NORETHINDRONE vs NORVIR