The Safety Rates Drug Report

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Drug     Injury     Quarter    

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
103755992 10375599 2 F 2016 20160324 20140811 20160331 EXP US-GLAXOSMITHKLINE-A1040849A GLAXOSMITHKLINE 0.00 M Y 0.00000 20160331 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
103755992 10375599 1 PS REQUIP XL ROPINIROLE HYDROCHLORIDE 1 Oral 8 MG AND 12 MG TABLETS OR 20 MG ONCE DAILY UNKNOWN 22008 20 MG PROLONGED-RELEASE TABLET QD
103755992 10375599 2 C TYLENOL WITH CODEINE ACETAMINOPHENCODEINE PHOSPHATE 1 0
103755992 10375599 3 C ELAVIL AMITRIPTYLINE HYDROCHLORIDE 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
103755992 10375599 1 Parkinson's disease

Outcome of event

Event ID CASEID OUTC COD
103755992 10375599 HO
103755992 10375599 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
103755992 10375599 Balance disorder
103755992 10375599 Computerised tomogram
103755992 10375599 Dehydration
103755992 10375599 Diverticulitis
103755992 10375599 Fall
103755992 10375599 Parkinsonism
103755992 10375599 Weight 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
103755992 10375599 1 20100817 0