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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 UNSPECIFIED INGREDIENT Cause Tendon rupture? 31 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 31 reports of Tendon rupture have been filed in association with UNSPECIFIED INGREDIENT. This represents 0.1% of all adverse event reports for UNSPECIFIED INGREDIENT.

31
Reports of Tendon rupture with UNSPECIFIED INGREDIENT
0.1%
of all UNSPECIFIED INGREDIENT reports
0
Deaths
16
Hospitalizations

How Dangerous Is Tendon rupture From UNSPECIFIED INGREDIENT?

Of the 31 reports, 16 (51.6%) required hospitalization, and 1 (3.2%) were considered life-threatening.

Is Tendon rupture Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for UNSPECIFIED INGREDIENT. However, 31 reports have been filed with the FAERS database.

What Other Side Effects Does UNSPECIFIED INGREDIENT Cause?

Death (2,090) Off label use (1,306) Drug ineffective (1,227) Completed suicide (1,190) Nausea (1,041) Fatigue (1,020) Dyspnoea (934) Pneumonia (903) Asthenia (894) Vomiting (877)

What Other Drugs Cause Tendon rupture?

LEVOFLOXACIN (1,321) ADALIMUMAB (1,124) CIPROFLOXACIN (880) ETANERCEPT (257) SIMVASTATIN (252) PREDNISONE (239) METHOTREXATE (238) ATORVASTATIN (205) UPADACITINIB (178) TOFACITINIB (169)

Which UNSPECIFIED INGREDIENT Alternatives Have Lower Tendon rupture Risk?

UNSPECIFIED INGREDIENT vs UPADACITINIB UNSPECIFIED INGREDIENT vs URAPIDIL UNSPECIFIED INGREDIENT vs UREA UNSPECIFIED INGREDIENT vs URIDINE TRIACETATE UNSPECIFIED INGREDIENT vs UROFOLLITROPIN

Related Pages

UNSPECIFIED INGREDIENT Full Profile All Tendon rupture Reports All Drugs Causing Tendon rupture UNSPECIFIED INGREDIENT Demographics