Does ESOMEPRAZOLE Cause Haemoglobin increased? 14 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 14 reports of Haemoglobin increased have been filed in association with ESOMEPRAZOLE (Esomeprazole Magnesium). This represents 0.0% of all adverse event reports for ESOMEPRAZOLE.
14
Reports of Haemoglobin increased with ESOMEPRAZOLE
0.0%
of all ESOMEPRAZOLE reports
10
Deaths
12
Hospitalizations
How Dangerous Is Haemoglobin increased From ESOMEPRAZOLE?
Of the 14 reports, 10 (71.4%) resulted in death, 12 (85.7%) required hospitalization, and 11 (78.6%) were considered life-threatening.
Is Haemoglobin increased Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ESOMEPRAZOLE. However, 14 reports have been filed with the FAERS database.
What Other Side Effects Does ESOMEPRAZOLE Cause?
Chronic kidney disease (35,281)
Acute kidney injury (18,678)
Renal failure (14,633)
End stage renal disease (10,231)
Renal injury (9,440)
Gastrooesophageal reflux disease (4,746)
Drug ineffective (4,420)
Tubulointerstitial nephritis (4,024)
Off label use (3,180)
Pain (2,898)
What Other Drugs Cause Haemoglobin increased?
RUXOLITINIB (332)
TREPROSTINIL (245)
SOTATERCEPT (151)
CLOZAPINE (142)
SOTATERCEPT-CSRK (100)
DARBEPOETIN ALFA (99)
TESTOSTERONE (96)
METFORMIN (93)
VOXELOTOR (86)
ROSUVASTATIN (85)
Which ESOMEPRAZOLE Alternatives Have Lower Haemoglobin increased Risk?
ESOMEPRAZOLE vs ESOMEPRAZOLE\ESOMEPRAZOLE\ESOMEPRAZOLE
ESOMEPRAZOLE vs ESOMEPRAZOLE\NAPROXEN
ESOMEPRAZOLE vs ESTAZOLAM
ESOMEPRAZOLE vs ESTRADIOL
ESOMEPRAZOLE vs ESTRADIOL CYPIONATE