Does FERRIC CARBOXYMALTOSE Cause Incorrect product administration duration? 19 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 19 reports of Incorrect product administration duration have been filed in association with FERRIC CARBOXYMALTOSE (Injectafer). This represents 0.2% of all adverse event reports for FERRIC CARBOXYMALTOSE.
19
Reports of Incorrect product administration duration with FERRIC CARBOXYMALTOSE
0.2%
of all FERRIC CARBOXYMALTOSE reports
0
Deaths
3
Hospitalizations
How Dangerous Is Incorrect product administration duration From FERRIC CARBOXYMALTOSE?
Of the 19 reports, 3 (15.8%) required hospitalization, and 2 (10.5%) were considered life-threatening.
Is Incorrect product administration duration Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for FERRIC CARBOXYMALTOSE. However, 19 reports have been filed with the FAERS database.
What Other Side Effects Does FERRIC CARBOXYMALTOSE Cause?
Hypophosphataemia (1,046)
Nausea (874)
Dyspnoea (737)
Headache (594)
Dizziness (528)
Pain (511)
Urticaria (509)
Pruritus (486)
Maternal exposure during pregnancy (468)
Vomiting (396)
What Other Drugs Cause Incorrect product administration duration?
ETONOGESTREL (3,974)
POLYETHYLENE GLYCOL 3350 (2,129)
NIRMATRELVIR\RITONAVIR (744)
DOCOSANOL (634)
LANSOPRAZOLE (564)
LOPERAMIDE (543)
NAPROXEN (499)
INSULIN LISPRO (479)
DICLOFENAC (362)
OMEPRAZOLE (302)
Which FERRIC CARBOXYMALTOSE Alternatives Have Lower Incorrect product administration duration Risk?
FERRIC CARBOXYMALTOSE vs FERRIC DERISOMALTOSE
FERRIC CARBOXYMALTOSE vs FERRIC HYDROXIDE
FERRIC CARBOXYMALTOSE vs FERRIC MALTOL
FERRIC CARBOXYMALTOSE vs FERRIC OXYHYDROXIDE
FERRIC CARBOXYMALTOSE vs FERROUS