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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.

PureTek Corporation: 3 Drugs and 274 Adverse Event Reports

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PureTek Corporation manufactures 3 drugs with a combined 274 adverse event reports in the FDA FAERS database. Their most reported drug is CALCIUM PANTOTHENATE.

3
Drugs
274
Combined Reports
41
Total Deaths
66
Total Hospitalizations

All PureTek Corporation Drugs & Safety Profiles

Drug Brand Name Reports Deaths Death Rate Hosp.
CALCIUM PANTOTHENATE Dexatran 204 41 20.1% 58
LEVOMEFOLATE Folixate 49 0 N/A 7
CAPSICUM OLEORESIN Circatrix 21 0 N/A 1