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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 SEMAGLUTIDE Cause Hyperkeratosis? 8 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 8 reports of Hyperkeratosis have been filed in association with SEMAGLUTIDE (WEGOVY). This represents 0.0% of all adverse event reports for SEMAGLUTIDE.

8
Reports of Hyperkeratosis with SEMAGLUTIDE
0.0%
of all SEMAGLUTIDE reports
0
Deaths
2
Hospitalizations

How Dangerous Is Hyperkeratosis From SEMAGLUTIDE?

Of the 8 reports, 2 (25.0%) required hospitalization.

Is Hyperkeratosis Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for SEMAGLUTIDE. However, 8 reports have been filed with the FAERS database.

What Other Side Effects Does SEMAGLUTIDE Cause?

Nausea (10,036) Vomiting (6,518) Off label use (5,425) Diarrhoea (5,331) Decreased appetite (4,317) Constipation (4,036) Weight decreased (3,518) Impaired gastric emptying (2,622) Product use in unapproved indication (2,613) Wrong technique in product usage process (2,538)

What Other Drugs Cause Hyperkeratosis?

CABOZANTINIB S-MALATE (411) ADALIMUMAB (332) SUNITINIB MALATE (170) ETANERCEPT (168) SORAFENIB (150) METHOTREXATE (149) VEMURAFENIB (145) REGORAFENIB (136) RIPRETINIB (124) RITUXIMAB (121)

Which SEMAGLUTIDE Alternatives Have Lower Hyperkeratosis Risk?

SEMAGLUTIDE vs SEMUSTINE SEMAGLUTIDE vs SENNA LEAF SEMAGLUTIDE vs SENNA LEAF\SENNOSIDES\SENNOSIDES A AND B SEMAGLUTIDE vs SENNOSIDES SEMAGLUTIDE vs SENNOSIDES A AND B

Related Pages

SEMAGLUTIDE Full Profile All Hyperkeratosis Reports All Drugs Causing Hyperkeratosis SEMAGLUTIDE Demographics