Does CEFOPERAZONE\SULBACTAM Cause Haemoglobin decreased? 23 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 23 reports of Haemoglobin decreased have been filed in association with CEFOPERAZONE\SULBACTAM. This represents 2.9% of all adverse event reports for CEFOPERAZONE\SULBACTAM.
23
Reports of Haemoglobin decreased with CEFOPERAZONE\SULBACTAM
2.9%
of all CEFOPERAZONE\SULBACTAM reports
1
Deaths
11
Hospitalizations
How Dangerous Is Haemoglobin decreased From CEFOPERAZONE\SULBACTAM?
Of the 23 reports, 1 (4.3%) resulted in death, 11 (47.8%) required hospitalization, and 7 (30.4%) were considered life-threatening.
Is Haemoglobin decreased Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for CEFOPERAZONE\SULBACTAM. However, 23 reports have been filed with the FAERS database.
What Other Side Effects Does CEFOPERAZONE\SULBACTAM Cause?
Off label use (155)
Drug ineffective (88)
Coagulopathy (62)
Platelet count decreased (59)
Hepatic function abnormal (57)
Drug-induced liver injury (39)
Condition aggravated (38)
Pyrexia (34)
Diarrhoea (32)
Pruritus (31)
What Other Drugs Cause Haemoglobin decreased?
LENALIDOMIDE (4,031)
RUXOLITINIB (3,297)
ECULIZUMAB (3,028)
ADALIMUMAB (2,459)
CLOZAPINE (2,396)
RITUXIMAB (1,803)
APIXABAN (1,779)
NIRAPARIB (1,759)
METHOTREXATE (1,754)
RIBAVIRIN (1,753)
Which CEFOPERAZONE\SULBACTAM Alternatives Have Lower Haemoglobin decreased Risk?
CEFOPERAZONE\SULBACTAM vs CEFOTAXIME
CEFOPERAZONE\SULBACTAM vs CEFOXITIN
CEFOPERAZONE\SULBACTAM vs CEFPODOXIME
CEFOPERAZONE\SULBACTAM vs CEFPODOXIME PROXETIL
CEFOPERAZONE\SULBACTAM vs CEFPROZIL