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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 TIQUIZIUM Cause Intentional product misuse? 7 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 7 reports of Intentional product misuse have been filed in association with TIQUIZIUM. This represents 41.2% of all adverse event reports for TIQUIZIUM.

7
Reports of Intentional product misuse with TIQUIZIUM
41.2%
of all TIQUIZIUM reports
0
Deaths
1
Hospitalizations

How Dangerous Is Intentional product misuse From TIQUIZIUM?

Of the 7 reports, 1 (14.3%) required hospitalization.

Is Intentional product misuse Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for TIQUIZIUM. However, 7 reports have been filed with the FAERS database.

What Other Side Effects Does TIQUIZIUM Cause?

Abdominal discomfort (8) Drug hypersensitivity (8) Arthritis (6) Barrett's oesophagus (6) Bladder disorder (6) Blood magnesium decreased (6) Blood zinc decreased (6) Condition aggravated (6) Cystitis (6) Diabetes mellitus (6)

What Other Drugs Cause Intentional product misuse?

ETANERCEPT (3,992) PREGABALIN (3,731) BUDESONIDE\FORMOTEROL (3,399) ACETAMINOPHEN (2,924) ESOMEPRAZOLE (2,852) MINOXIDIL (2,418) TOFACITINIB (2,331) CINACALCET (2,092) QUETIAPINE (1,855) ALPRAZOLAM (1,709)

Related Pages

TIQUIZIUM Full Profile All Intentional product misuse Reports All Drugs Causing Intentional product misuse TIQUIZIUM Demographics