Does PAMIDRONATE Cause Excessive granulation tissue? 11 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 11 reports of Excessive granulation tissue have been filed in association with PAMIDRONATE (Pamidronate Disodium). This represents 0.7% of all adverse event reports for PAMIDRONATE.
11
Reports of Excessive granulation tissue with PAMIDRONATE
0.7%
of all PAMIDRONATE reports
3
Deaths
4
Hospitalizations
How Dangerous Is Excessive granulation tissue From PAMIDRONATE?
Of the 11 reports, 3 (27.3%) resulted in death, 4 (36.4%) 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 PAMIDRONATE. However, 11 reports have been filed with the FAERS database.
What Other Side Effects Does PAMIDRONATE Cause?
Osteonecrosis of jaw (313)
Drug ineffective (180)
Pain (164)
Off label use (143)
Pyrexia (106)
Malignant neoplasm progression (103)
Dyspnoea (102)
Fatigue (97)
Pain in jaw (97)
Metastases to bone (95)
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)
PREDNISONE (11)
Which PAMIDRONATE Alternatives Have Lower Excessive granulation tissue Risk?
PAMIDRONATE vs PAMIDRONIC ACID
PAMIDRONATE vs PANCRELIPASE
PAMIDRONATE vs PANCRELIPASE AMYLASE\PANCRELIPASE LIPASE\PANCRELIPASE PROTEASE
PAMIDRONATE vs PANCURONIUM
PAMIDRONATE vs PANITUMUMAB