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
122865622 12286562 2 F 201012 20160809 20160420 20160815 EXP DE-BFARM-16121925 DE-009507513-1604DEU010016 MERCK 63.00 YR M Y 114.00000 KG 20160815 OT DE DE

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
122865622 12286562 1 PS SIMVASTATIN. SIMVASTATIN 1 Oral 40 MG, ONCE A DAY Y U 19766 40 MG TABLET QD
122865622 12286562 2 SS FLUVASTATIN SODIUM. FLUVASTATIN SODIUM 1 Oral 40 MG, ONCE A DAY Y 0 40 MG TABLET QD
122865622 12286562 3 SS ATORVASTATIN ATORVASTATIN 1 Oral 40 MG, ONCE A DAY Y 0 40 MG TABLET QD
122865622 12286562 4 SS ATORVASTATIN ATORVASTATIN 1 Y 0 TABLET

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
122865622 12286562 1 Hypercholesterolaemia
122865622 12286562 2 Hypercholesterolaemia
122865622 12286562 3 Coronary artery disease
122865622 12286562 4 Hypercholesterolaemia

Outcome of event

Event ID CASEID OUTC COD
122865622 12286562 HO
122865622 12286562 OT
122865622 12286562 DS
122865622 12286562 LT

Reactions reported

Event ID CASEID DRUG REC ACT PT
122865622 12286562 Alveolitis
122865622 12286562 Atypical pneumonia
122865622 12286562 Dyspnoea
122865622 12286562 Dyspnoea at rest
122865622 12286562 Myopathy
122865622 12286562 Tendon rupture
122865622 12286562 Walking disability

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
122865622 12286562 1 201010 0
122865622 12286562 2 201010 201012 0
122865622 12286562 3 201306 201308 0