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
125690001 12569000 1 I 20160625 20160711 20160719 20160719 EXP GB-ASTRAZENECA-2016SE75079 ASTRAZENECA 67.00 YR F Y 62.60000 KG 20160719 CN 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
125690001 12569000 1 PS ROSUVASTATIN CALCIUM. ROSUVASTATIN CALCIUM 1 Oral 5.0MG UNKNOWN U U 21366 5 MG TABLET
125690001 12569000 2 C PRAVASTATIN. PRAVASTATIN 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125690001 12569000 1 Type IIa hyperlipidaemia

Outcome of event

Event ID CASEID OUTC COD
125690001 12569000 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125690001 12569000 Cardiac flutter
125690001 12569000 Dyspnoea
125690001 12569000 Muscle spasms
125690001 12569000 Muscle twitching
125690001 12569000 Muscular weakness
125690001 12569000 Musculoskeletal stiffness
125690001 12569000 Myalgia
125690001 12569000 Pain

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
125690001 12569000 1 20160622 0