Does DICLOFENAC Cause Hyperkalaemia? 321 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 321 reports of Hyperkalaemia have been filed in association with DICLOFENAC (Diclofenac Sodium Delayed Release). This represents 0.4% of all adverse event reports for DICLOFENAC.
321
Reports of Hyperkalaemia with DICLOFENAC
0.4%
of all DICLOFENAC reports
11
Deaths
217
Hospitalizations
How Dangerous Is Hyperkalaemia From DICLOFENAC?
Of the 321 reports, 11 (3.4%) resulted in death, 217 (67.6%) required hospitalization, and 61 (19.0%) were considered life-threatening.
Is Hyperkalaemia Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for DICLOFENAC. However, 321 reports have been filed with the FAERS database.
What Other Side Effects Does DICLOFENAC Cause?
Drug ineffective (24,885)
Product use in unapproved indication (12,197)
Off label use (10,370)
Pain (9,276)
Product use issue (8,009)
Fatigue (7,908)
Rash (7,852)
Rheumatoid arthritis (7,366)
Abdominal discomfort (7,257)
Product administered at inappropriate site (6,919)
What Other Drugs Cause Hyperkalaemia?
METFORMIN (2,565)
SPIRONOLACTONE (2,518)
FUROSEMIDE (2,035)
RAMIPRIL (1,383)
SACUBITRIL\VALSARTAN (1,192)
SULFAMETHOXAZOLE\TRIMETHOPRIM (1,036)
LISINOPRIL (948)
POTASSIUM (944)
BISOPROLOL (850)
TACROLIMUS (713)
Which DICLOFENAC Alternatives Have Lower Hyperkalaemia Risk?
DICLOFENAC vs DICLOFENAC DIETHYLAMINE
DICLOFENAC vs DICLOFENAC EPOLAMINE
DICLOFENAC vs DICLOFENAC\DICLOFENAC
DICLOFENAC vs DICLOFENAC\MISOPROSTOL
DICLOFENAC vs DICLOXACILLIN