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Important: This site presents data from the FDA Adverse Event Reporting System (FAERS). A report does not mean the drug caused the event. Full disclaimer.

Does TELMISARTAN Cause Poor quality product administered? 8 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 8 reports of Poor quality product administered have been filed in association with TELMISARTAN (telmisartan). This represents 0.1% of all adverse event reports for TELMISARTAN.

8
Reports of Poor quality product administered with TELMISARTAN
0.1%
of all TELMISARTAN reports
0
Deaths
0
Hospitalizations

How Dangerous Is Poor quality product administered From TELMISARTAN?

Of the 8 reports.

Is Poor quality product administered Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for TELMISARTAN. However, 8 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 Poor quality product administered?

ONABOTULINUMTOXINA (495) ICOSAPENT ETHYL (452) MINOXIDIL (428) TUBERCULIN PURIFIED PROTEIN DERIVATIVE (376) ADALIMUMAB (239) TESTOSTERONE CYPIONATE (235) SOMATROPIN (234) POLYETHYLENE GLYCOL 3350 (223) IBUPROFEN (222) INSULIN GLARGINE (133)

Which TELMISARTAN Alternatives Have Lower Poor quality product administered Risk?

TELMISARTAN vs TELOTRISTAT ETHYL TELMISARTAN vs TEMAZEPAM TELMISARTAN vs TEMODAR TELMISARTAN vs TEMOZOLOMIDE TELMISARTAN vs TEMSIROLIMUS

Related Pages

TELMISARTAN Full Profile All Poor quality product administered Reports All Drugs Causing Poor quality product administered TELMISARTAN Demographics