Does TELMISARTAN Cause Wrong technique in product usage process? 113 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 113 reports of Wrong technique in product usage process have been filed in association with TELMISARTAN (telmisartan). This represents 1.9% of all adverse event reports for TELMISARTAN.
113
Reports of Wrong technique in product usage process with TELMISARTAN
1.9%
of all TELMISARTAN reports
0
Deaths
2
Hospitalizations
How Dangerous Is Wrong technique in product usage process From TELMISARTAN?
Of the 113 reports, 2 (1.8%) required hospitalization, and 1 (0.9%) were considered life-threatening.
Is Wrong technique in product usage process Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for TELMISARTAN. However, 113 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 Wrong technique in product usage process?
EVOLOCUMAB (21,664)
ALBUTEROL (17,114)
ADALIMUMAB (11,766)
PEGFILGRASTIM (10,217)
ETANERCEPT (9,835)
ERENUMAB-AOOE (9,359)
SACUBITRIL\VALSARTAN (8,022)
LEUPROLIDE (5,062)
FENTANYL (2,812)
SEMAGLUTIDE (2,538)
Which TELMISARTAN Alternatives Have Lower Wrong technique in product usage process Risk?
TELMISARTAN vs TELOTRISTAT ETHYL
TELMISARTAN vs TEMAZEPAM
TELMISARTAN vs TEMODAR
TELMISARTAN vs TEMOZOLOMIDE
TELMISARTAN vs TEMSIROLIMUS