Does NITROFURANTOIN Cause Recalled product administered? 7 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 7 reports of Recalled product administered have been filed in association with NITROFURANTOIN (Nitrofurantoin Macrocrystals). This represents 0.1% of all adverse event reports for NITROFURANTOIN.
7
Reports of Recalled product administered with NITROFURANTOIN
0.1%
of all NITROFURANTOIN reports
0
Deaths
0
Hospitalizations
How Dangerous Is Recalled product administered From NITROFURANTOIN?
Of the 7 reports.
Is Recalled product administered Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for NITROFURANTOIN. However, 7 reports have been filed with the FAERS database.
What Other Side Effects Does NITROFURANTOIN Cause?
Drug hypersensitivity (562)
Dyspnoea (442)
Nausea (401)
Fatigue (378)
Rash (371)
Malaise (364)
Vomiting (358)
Headache (335)
Pyrexia (321)
Dizziness (312)
What Other Drugs Cause Recalled product administered?
RAMIPRIL (1,028)
LISINOPRIL (744)
PENICILLIN G BENZATHINE (500)
LEVOTHYROXINE (406)
HUMAN IMMUNOGLOBULIN G (382)
VARENICLINE (381)
VALSARTAN (267)
QUINAPRIL (243)
TRIAMCINOLONE ACETONIDE (222)
RANITIDINE (204)
Which NITROFURANTOIN Alternatives Have Lower Recalled product administered Risk?
NITROFURANTOIN vs NITROFURANTOIN\NITROFURANTOIN
NITROFURANTOIN vs NITROFURAZONE
NITROFURANTOIN vs NITROGLYCERIN
NITROFURANTOIN vs NITROUS
NITROFURANTOIN vs NITROUS\OXYGEN