CARBIDOPA AND LEVODOPA

Generic: CARBIDOPA AND LEVODOPA

Dr. Reddy's Laboratories IncManufacturer
ORALRoute
CARBIDOPAActive Substance
1992-08-28Original Approval

CARBIDOPA AND LEVODOPA is FDA application ANDA073607, sponsored by DR REDDYS LABS SA. Any recalls listed below come from FDA drug enforcement reports, and reaction counts are the number of FAERS adverse event reports that mention the drug and that reaction; a report does not prove the drug caused it.

Recalls

Class II2017-01-12
Sun Pharma Carbidopa and Levodopa Tablets USP 25 mg/250 mg a) 100-count bottles (NDC 62756-519-88), b) 500-count bottles

Failed Dissolution Specifications

Top Reported Reactions

1
DRUG INEFFECTIVE
589 reports
2
FALL
428 reports
3
HALLUCINATION
407 reports
4
DYSKINESIA
355 reports
5
TREMOR
310 reports
6
COUGH
261 reports
7
DEATH
248 reports
8
DIZZINESS
244 reports
9
NAUSEA
244 reports
10
GAIT DISTURBANCE
240 reports