Does TELMISARTAN Cause Haemoglobin decreased? 105 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 105 reports of Haemoglobin decreased have been filed in association with TELMISARTAN (telmisartan). This represents 1.8% of all adverse event reports for TELMISARTAN.
105
Reports of Haemoglobin decreased with TELMISARTAN
1.8%
of all TELMISARTAN reports
4
Deaths
97
Hospitalizations
How Dangerous Is Haemoglobin decreased From TELMISARTAN?
Of the 105 reports, 4 (3.8%) resulted in death, 97 (92.4%) required hospitalization, and 2 (1.9%) 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 TELMISARTAN. However, 105 reports have been filed with the FAERS database.
What Other Side Effects Does TELMISARTAN Cause?
Drug ineffective (685)
Dizziness (569)
Dyspnoea (556)
Headache (508)
Fall (500)
Nausea (486)
Hypertension (477)
Blood pressure increased (473)
Diarrhoea (467)
Malaise (458)
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 TELMISARTAN Alternatives Have Lower Haemoglobin decreased Risk?
TELMISARTAN vs TELOTRISTAT ETHYL
TELMISARTAN vs TEMAZEPAM
TELMISARTAN vs TEMODAR
TELMISARTAN vs TEMOZOLOMIDE
TELMISARTAN vs TEMSIROLIMUS