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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 RISEDRONATE Cause Hyperkeratosis? 5 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 5 reports of Hyperkeratosis have been filed in association with RISEDRONATE (Risedronate Sodium). This represents 0.1% of all adverse event reports for RISEDRONATE.

5
Reports of Hyperkeratosis with RISEDRONATE
0.1%
of all RISEDRONATE reports
0
Deaths
4
Hospitalizations

How Dangerous Is Hyperkeratosis From RISEDRONATE?

Of the 5 reports, 4 (80.0%) required hospitalization.

Is Hyperkeratosis Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for RISEDRONATE. However, 5 reports have been filed with the FAERS database.

What Other Side Effects Does RISEDRONATE Cause?

Drug hypersensitivity (1,124) Asthma (1,087) Pain (973) Vomiting (971) Drug ineffective (919) Dyspnoea (898) Pneumonia (807) Wheezing (772) Oedema (708) Malaise (668)

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 RISEDRONATE Alternatives Have Lower Hyperkeratosis Risk?

RISEDRONATE vs RISEDRONIC ACID RISEDRONATE vs RISPERDAL RISEDRONATE vs RISPERDAL CONSTA RISEDRONATE vs RISPERIDONE RISEDRONATE vs RITALIN

Related Pages

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