Does IBUPROFEN Cause Recalled product? 8 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 8 reports of Recalled product have been filed in association with IBUPROFEN (equate ibuprofen). This represents 0.0% of all adverse event reports for IBUPROFEN.
8
Reports of Recalled product with IBUPROFEN
0.0%
of all IBUPROFEN reports
0
Deaths
0
Hospitalizations
How Dangerous Is Recalled product From IBUPROFEN?
Of the 8 reports.
Is Recalled product Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for IBUPROFEN. However, 8 reports have been filed with the FAERS database.
What Other Side Effects Does IBUPROFEN Cause?
Drug ineffective (9,352)
Drug hypersensitivity (5,269)
Nausea (4,129)
Vomiting (4,116)
Acute kidney injury (3,639)
Product use in unapproved indication (3,596)
Toxicity to various agents (3,584)
Off label use (3,556)
Intentional overdose (3,185)
Headache (3,010)
What Other Drugs Cause Recalled product?
PARATHYROID HORMONE (900)
ANTIHEMOPHILIC FACTOR, HUMAN RECOMBINANT (80)
CALCITRIOL (68)
CALCIUM (66)
REMDESIVIR (36)
LEVOTHYROXINE\LIOTHYRONINE (34)
TESTOSTERONE (32)
VALSARTAN (32)
CHLORHEXIDINE (28)
ALCOHOL (26)
Which IBUPROFEN Alternatives Have Lower Recalled product Risk?
IBUPROFEN vs IBUPROFEN LYSINE
IBUPROFEN vs IBUPROFEN UNKNOWN PRODUCT
IBUPROFEN vs IBUPROFEN\IBUPROFEN
IBUPROFEN vs IBUPROFEN\PHENYLEPHRINE
IBUPROFEN vs IBUPROFEN\PSEUDOEPHEDRINE