The Safety Rates Drug Report

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Person who experienced the adverse event (patient)

Event ID CASEID CASEVERSION I F COD EVENT DT MFR DT INIT FDA DT FDA DT REPT COD AUTH NUM MFR NUM MFR SNDR LIT REF AGE AGE COD AGE GRP GNDR COD E SUB WT WT COD REPT DT TO MFR OCCP COD REPORTER COUNTRY OCCR COUNTRY
107865152 10786515 2 F 20160906 20150211 20160908 PER US-GLAXOSMITHKLINE-A1075097A GLAXOSMITHKLINE 0.00 F Y 0.00000 20160908 CN US US

Drug(s) used by person

Event ID CASEID DRUG SEQ ROLE COD DRUGNAME PROD AI VAL VBM ROUTE DOSE VBM CUM DOSE CHR CUM DOSE UNIT DECHAL RECHAL LOT NUM EXP DT NDA NUM DOSE AMT DOSE UNIT DOSE FORM DOSE FREQ
107865152 10786515 1 PS Ropinirole Tablet ROPINIROLE 1 Oral PATIENT REPORTED SHE TAKES 2 MG THREE TIMES PER DAY AT MORNING, LUNCH AND EVENING, AND HER PHYS[...] N UNKNOWN 20658 TABLET
107865152 10786515 2 SS Ropinirole Tablet ROPINIROLE 1 4 MG, UNK N UNKNOWN 20658 4 MG TABLET
107865152 10786515 3 SS REQUIP ROPINIROLE HYDROCHLORIDE 1 Oral PATIENT REPORTED SHE TAKES 2 MG THREE TIMES PER DAY AT MORNING, LUNCH AND EVENING, AND HER PHYS[...] U UNKNOWN 20658 TABLET
107865152 10786515 4 C STALEVO CARBIDOPAENTACAPONELEVODOPA 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
107865152 10786515 1 Parkinson's disease
107865152 10786515 3 Parkinson's disease

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
107865152 10786515 Asthenia
107865152 10786515 Drug ineffective
107865152 10786515 Gait disturbance
107865152 10786515 Osteoporosis
107865152 10786515 Product substitution issue
107865152 10786515 Therapeutic response decreased

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

Event ID CASEID DSG DRUG SEQ START DT END DT DUR DUR COD
107865152 10786515 2 1997 0