Does IBUPROFEN Cause Product administration error? 211 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 211 reports of Product administration error have been filed in association with IBUPROFEN (equate ibuprofen). This represents 0.2% of all adverse event reports for IBUPROFEN.
211
Reports of Product administration error with IBUPROFEN
0.2%
of all IBUPROFEN reports
19
Deaths
129
Hospitalizations
How Dangerous Is Product administration error From IBUPROFEN?
Of the 211 reports, 19 (9.0%) resulted in death, 129 (61.1%) required hospitalization, and 19 (9.0%) were considered life-threatening.
Is Product administration error Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for IBUPROFEN. However, 211 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 Product administration error?
HYDROXYPROGESTERONE CAPROATE (972)
ACETAMINOPHEN (666)
CENEGERMIN-BKBJ (613)
LEUPROLIDE (595)
EVOLOCUMAB (565)
ADALIMUMAB (543)
METHYLPHENIDATE (414)
OLMESARTAN MEDOXOMIL (314)
ASPIRIN (241)
SECUKINUMAB (225)
Which IBUPROFEN Alternatives Have Lower Product administration error Risk?
IBUPROFEN vs IBUPROFEN LYSINE
IBUPROFEN vs IBUPROFEN UNKNOWN PRODUCT
IBUPROFEN vs IBUPROFEN\IBUPROFEN
IBUPROFEN vs IBUPROFEN\PHENYLEPHRINE
IBUPROFEN vs IBUPROFEN\PSEUDOEPHEDRINE