Does SORBITOL Cause Excessive granulation tissue? 6 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 6 reports of Excessive granulation tissue have been filed in association with SORBITOL (Plaque identifying). This represents 8.2% of all adverse event reports for SORBITOL.
6
Reports of Excessive granulation tissue with SORBITOL
8.2%
of all SORBITOL reports
1
Deaths
1
Hospitalizations
How Dangerous Is Excessive granulation tissue From SORBITOL?
Of the 6 reports, 1 (16.7%) resulted in death, 1 (16.7%) required hospitalization.
Is Excessive granulation tissue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for SORBITOL. However, 6 reports have been filed with the FAERS database.
What Other Side Effects Does SORBITOL Cause?
Diarrhoea (8)
Colitis (7)
Crystal deposit intestine (7)
Disorientation (7)
Decreased appetite (6)
Erythema (6)
Irritability (6)
Oedema (6)
Peripheral swelling (6)
Skin disorder (6)
What Other Drugs Cause Excessive granulation tissue?
CARBIDOPA\LEVODOPA (117)
ADALIMUMAB (38)
BACLOFEN (31)
ZOLEDRONIC ACID (29)
ZOMETA (27)
AREDIA (21)
METHOTREXATE (19)
RITUXIMAB (13)
BECAPLERMIN (11)
PAMIDRONATE (11)