Does KETOPROFEN Cause Shock haemorrhagic? 19 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 19 reports of Shock haemorrhagic have been filed in association with KETOPROFEN (Orudis). This represents 0.3% of all adverse event reports for KETOPROFEN.
19
Reports of Shock haemorrhagic with KETOPROFEN
0.3%
of all KETOPROFEN reports
3
Deaths
10
Hospitalizations
How Dangerous Is Shock haemorrhagic From KETOPROFEN?
Of the 19 reports, 3 (15.8%) resulted in death, 10 (52.6%) required hospitalization, and 10 (52.6%) were considered life-threatening.
Is Shock haemorrhagic Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for KETOPROFEN. However, 19 reports have been filed with the FAERS database.
What Other Side Effects Does KETOPROFEN Cause?
Pain (595)
Headache (574)
Hypersensitivity (556)
Erythema (546)
Acute kidney injury (517)
Hyperhidrosis (516)
Hepatic enzyme increased (508)
Asthma (507)
Rheumatoid arthritis (493)
Immunodeficiency (492)
What Other Drugs Cause Shock haemorrhagic?
RIVAROXABAN (906)
ASPIRIN (830)
APIXABAN (476)
ENOXAPARIN (473)
CLOPIDOGREL BISULFATE (403)
DABIGATRAN ETEXILATE (383)
WARFARIN (351)
HEPARIN (291)
TACROLIMUS (241)
FUROSEMIDE (204)
Which KETOPROFEN Alternatives Have Lower Shock haemorrhagic Risk?
KETOPROFEN vs KETOPROFEN LYSINE
KETOPROFEN vs KETOROLAC TROMETHAMINE
KETOPROFEN vs KETOROLAC\KETOROLAC TROMETHAMINE
KETOPROFEN vs KETOTIFEN
KETOPROFEN vs KLONOPIN