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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 SOTATERCEPT Cause Device dislocation? 11 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 11 reports of Device dislocation have been filed in association with SOTATERCEPT. This represents 1.1% of all adverse event reports for SOTATERCEPT.

11
Reports of Device dislocation with SOTATERCEPT
1.1%
of all SOTATERCEPT reports
0
Deaths
4
Hospitalizations

How Dangerous Is Device dislocation From SOTATERCEPT?

Of the 11 reports, 4 (36.4%) required hospitalization.

Is Device dislocation Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for SOTATERCEPT. However, 11 reports have been filed with the FAERS database.

What Other Side Effects Does SOTATERCEPT Cause?

Headache (214) Haemoglobin increased (151) Nausea (131) Diarrhoea (130) Epistaxis (130) Fatigue (125) Dizziness (109) Dyspnoea (84) Pericardial effusion (65) Vomiting (61)

What Other Drugs Cause Device dislocation?

LEVONORGESTREL (13,757) COPPER (6,955) CARBIDOPA\LEVODOPA (2,937) ETONOGESTREL (2,909) TREPROSTINIL (1,626) MIRENA (677) BACLOFEN (492) PARAGARD 380A (479) ADALIMUMAB (372) EPOPROSTENOL (358)

Which SOTATERCEPT Alternatives Have Lower Device dislocation Risk?

SOTATERCEPT vs SOTATERCEPT-CSRK SOTATERCEPT vs SOTORASIB SOTATERCEPT vs SOTROVIMAB SOTATERCEPT vs SOVALDI SOTATERCEPT vs SOYBEAN OIL

Related Pages

SOTATERCEPT Full Profile All Device dislocation Reports All Drugs Causing Device dislocation SOTATERCEPT Demographics