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
126960871 12696087 1 I 20130130 20160825 20160829 20160829 EXP IT-009507513-1608ITA013334 MERCK 50.00 YR F Y 0.00000 20160829 OT IT IT

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
126960871 12696087 1 PS SIMVASTATIN. SIMVASTATIN 1 Oral Y U 19766 TABLET
126960871 12696087 2 SS PRAVASTATIN. PRAVASTATIN 1 Y U 0
126960871 12696087 3 SS ATORVASTATIN ATORVASTATIN 1 Y U 0
126960871 12696087 4 SS ROSUVASTATIN CALCIUM. ROSUVASTATIN CALCIUM 1 Y U 0
126960871 12696087 5 C CARDIOASPIRIN ASPIRIN 1 U 0 TABLET
126960871 12696087 6 C BISOPROLOL FUMARATE. BISOPROLOL FUMARATE 1 U 0
126960871 12696087 7 C EZETIMIBE. EZETIMIBE 1 U 0 TABLET
126960871 12696087 8 C TELMISARTAN. TELMISARTAN 1 U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126960871 12696087 1 Myocardial infarction
126960871 12696087 2 Myocardial infarction
126960871 12696087 3 Myocardial infarction
126960871 12696087 4 Myocardial infarction

Outcome of event

Event ID CASEID OUTC COD
126960871 12696087 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126960871 12696087 Myopathy
126960871 12696087 Pain in extremity

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

no results found

Therapies reported

no results found