Does HEMIN Cause Product dose omission issue? 10 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 10 reports of Product dose omission issue have been filed in association with HEMIN (Panhematin). This represents 2.8% of all adverse event reports for HEMIN.
10
Reports of Product dose omission issue with HEMIN
2.8%
of all HEMIN reports
0
Deaths
3
Hospitalizations
How Dangerous Is Product dose omission issue From HEMIN?
Of the 10 reports, 3 (30.0%) required hospitalization.
Is Product dose omission issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for HEMIN. However, 10 reports have been filed with the FAERS database.
What Other Side Effects Does HEMIN Cause?
Off label use (105)
Phlebitis (30)
Device occlusion (21)
Nausea (19)
Pain (18)
Vomiting (17)
Abdominal pain (16)
Headache (16)
Porphyria acute (16)
Porphyria (14)
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 HEMIN Alternatives Have Lower Product dose omission issue Risk?
HEMIN vs HEPARIN
HEMIN vs HEPARIN\SODIUM
HEMIN vs HEPATITIS B VIRUS VACCINE
HEMIN vs HERBALS
HEMIN vs HERBALS\MITRAGYNINE