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
126990612 12699061 2 F 2015 20160920 20160830 20160923 EXP US-GLAXOSMITHKLINE-US2016GSK123287 GLAXOSMITHKLINE 0.00 F Y 54.42000 KG 20160923 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
126990612 12699061 1 PS REQUIP ROPINIROLE HYDROCHLORIDE 1 Y UNKNOWN 20658
126990612 12699061 2 SS SINEMET CARBIDOPALEVODOPA 1 U UNKNOWN 0
126990612 12699061 3 SS NUPLAZID PIMAVANSERIN TARTRATE 1 U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126990612 12699061 1 Product used for unknown indication
126990612 12699061 2 Parkinson's disease
126990612 12699061 3 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
126990612 12699061 OT
126990612 12699061 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
126990612 12699061 Condition aggravated
126990612 12699061 Depressed level of consciousness
126990612 12699061 Fatigue
126990612 12699061 Hypotension
126990612 12699061 Miosis

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

no results found

Therapies reported

no results found