Does IRON SUCROSE Cause Incorrect product administration duration? 106 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 106 reports of Incorrect product administration duration have been filed in association with IRON SUCROSE (Iron Sucrose). This represents 2.2% of all adverse event reports for IRON SUCROSE.
106
Reports of Incorrect product administration duration with IRON SUCROSE
2.2%
of all IRON SUCROSE reports
0
Deaths
12
Hospitalizations
How Dangerous Is Incorrect product administration duration From IRON SUCROSE?
Of the 106 reports, 12 (11.3%) required hospitalization, and 5 (4.7%) 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 IRON SUCROSE. However, 106 reports have been filed with the FAERS database.
What Other Side Effects Does IRON SUCROSE Cause?
Drug hypersensitivity (942)
Dyspnoea (548)
Nausea (530)
Pruritus (393)
Vomiting (344)
Urticaria (326)
Dizziness (284)
Hypotension (277)
Off label use (277)
Rash (259)
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 IRON SUCROSE Alternatives Have Lower Incorrect product administration duration Risk?
IRON SUCROSE vs IRON\VITAMINS
IRON SUCROSE vs ISATUXIMAB
IRON SUCROSE vs ISATUXIMAB-IRFC
IRON SUCROSE vs ISAVUCONAZOLE
IRON SUCROSE vs ISAVUCONAZONIUM