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
125957811 12595781 1 I 20131201 20160718 20160726 20160726 EXP GB-MHRA-EYC 00142377 PHHY2016GB098709 SANDOZ 72.00 YR F Y 66.67000 KG 20160726 OT GB GB

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
125957811 12595781 1 PS SIMVASTATIN. SIMVASTATIN 1 Oral 20 MG N U 77766 20 MG
125957811 12595781 2 SS SIMVASTATIN. SIMVASTATIN 1 Oral 40 MG N U 77766 40 MG
125957811 12595781 3 C INDERAL PROPRANOLOL HYDROCHLORIDE 1 Unknown U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125957811 12595781 1 Type IIa hyperlipidaemia
125957811 12595781 3 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
125957811 12595781 DS
125957811 12595781 HO
125957811 12595781 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125957811 12595781 Motor dysfunction
125957811 12595781 Muscle spasms
125957811 12595781 Myalgia

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
125957811 12595781 1 20130801 201309 0
125957811 12595781 2 20140101 0