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
127136801 12713680 1 I 20151110 20160830 20160904 20160904 EXP IT-009507513-1609ITA000520 MERCK 78.00 YR F Y 54.00000 KG 20160904 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
127136801 12713680 1 PS SIMVASTATIN. SIMVASTATIN 1 Y U 19766 TABLET
127136801 12713680 2 SS PRAVASTATIN. PRAVASTATIN 1 Y U 0
127136801 12713680 3 SS ATORVASTATIN ATORVASTATIN 1 Y U 0
127136801 12713680 4 SS ROSUVASTATIN CALCIUM. ROSUVASTATIN CALCIUM 1 Y U 0
127136801 12713680 5 SS LOVASTATIN. LOVASTATIN 1 U 0
127136801 12713680 6 C ZETIA EZETIMIBE 1 100 MG, UNK 0 100 MG TABLET
127136801 12713680 7 C LOPRESSOR METOPROLOL TARTRATE 1 0
127136801 12713680 8 C NORVASC AMLODIPINE BESYLATE 1 0
127136801 12713680 9 C PLAVIX CLOPIDOGREL BISULFATE 1 0
127136801 12713680 10 C IGROSELES ATENOLOLCHLORTHALIDONE 1 0
127136801 12713680 11 C RANITIDINE. RANITIDINE 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127136801 12713680 1 Dyslipidaemia
127136801 12713680 2 Dyslipidaemia
127136801 12713680 3 Dyslipidaemia
127136801 12713680 4 Dyslipidaemia
127136801 12713680 6 Dyslipidaemia
127136801 12713680 7 Hypertension
127136801 12713680 8 Hypertension
127136801 12713680 9 Carotid artery stenosis
127136801 12713680 10 Hypertension

Outcome of event

Event ID CASEID OUTC COD
127136801 12713680 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
127136801 12713680 Myopathy
127136801 12713680 Pain

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

no results found

Therapies reported

no results found