Does CORTICOTROPIN Cause Product dose omission issue? 528 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 528 reports of Product dose omission issue have been filed in association with CORTICOTROPIN (OHM Pituitarum Complex). This represents 4.5% of all adverse event reports for CORTICOTROPIN.
528
Reports of Product dose omission issue with CORTICOTROPIN
4.5%
of all CORTICOTROPIN reports
3
Deaths
116
Hospitalizations
How Dangerous Is Product dose omission issue From CORTICOTROPIN?
Of the 528 reports, 3 (0.6%) resulted in death, 116 (22.0%) required hospitalization, and 2 (0.4%) were considered life-threatening.
Is Product dose omission issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for CORTICOTROPIN. However, 528 reports have been filed with the FAERS database.
What Other Side Effects Does CORTICOTROPIN Cause?
Fatigue (1,032)
Drug ineffective (888)
Weight increased (781)
Injection site bruising (774)
Insomnia (724)
Headache (641)
Pain (635)
Malaise (591)
Peripheral swelling (589)
Dyspnoea (569)
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 CORTICOTROPIN Alternatives Have Lower Product dose omission issue Risk?
CORTICOTROPIN vs CORTISONE
CORTICOTROPIN vs CORTISONE\HYDROCORTISONE
CORTICOTROPIN vs COSMETICS
CORTICOTROPIN vs COUMADIN
CORTICOTROPIN vs COUMADIN TABS