Does KETOPROFEN Cause Haemodynamic instability? 8 Reports in FDA Database
Grow Your Own Natural Pharmacy at Home
Medicinal Garden Kit — 10 healing herbs, 4,818 seeds + step-by-step guide.
According to the FDA Adverse Event Reporting System (FAERS), 8 reports of Haemodynamic instability have been filed in association with KETOPROFEN (Orudis). This represents 0.1% of all adverse event reports for KETOPROFEN.
8
Reports of Haemodynamic instability with KETOPROFEN
0.1%
of all KETOPROFEN reports
1
Deaths
6
Hospitalizations
How Dangerous Is Haemodynamic instability From KETOPROFEN?
Of the 8 reports, 1 (12.5%) resulted in death, 6 (75.0%) required hospitalization, and 3 (37.5%) were considered life-threatening.
Is Haemodynamic instability Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for KETOPROFEN. However, 8 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 Haemodynamic instability?
METFORMIN (371)
AMLODIPINE (335)
TACROLIMUS (197)
DEXAMETHASONE (185)
ACETAMINOPHEN (184)
PROPOFOL (182)
VANCOMYCIN (171)
PREDNISONE (156)
MYCOPHENOLATE MOFETIL (142)
METHYLPREDNISOLONE (137)
Which KETOPROFEN Alternatives Have Lower Haemodynamic instability Risk?
KETOPROFEN vs KETOPROFEN LYSINE
KETOPROFEN vs KETOROLAC TROMETHAMINE
KETOPROFEN vs KETOROLAC\KETOROLAC TROMETHAMINE
KETOPROFEN vs KETOTIFEN
KETOPROFEN vs KLONOPIN