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
126977411 12697741 1 I 20121217 20160825 20160830 20160830 EXP IT-009507513-1608ITA013827 MERCK 63.00 YR F Y 62.00000 KG 20160830 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
126977411 12697741 1 PS SIMVASTATIN. SIMVASTATIN 1 UNK Y U 19766 FILM-COATED TABLET
126977411 12697741 2 SS PRAVASTATIN. PRAVASTATIN 1 UNK Y U 0
126977411 12697741 3 SS ATORVASTATIN ATORVASTATIN 1 UNK Y U 0
126977411 12697741 4 SS ROSUVASTATIN CALCIUM. ROSUVASTATIN CALCIUM 1 UNK Y U 0
126977411 12697741 5 C ASPIRIN. ASPIRIN 1 Oral UNK U 0 TABLET
126977411 12697741 6 C LOVASTATIN. LOVASTATIN 1 3 MG, UNK U 0 3 MG
126977411 12697741 7 C hydrochlorothiazide (+) valsartan HYDROCHLOROTHIAZIDEVALSARTAN 1 UNK U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126977411 12697741 1 Type II hyperlipidaemia
126977411 12697741 2 Type II hyperlipidaemia
126977411 12697741 3 Type II hyperlipidaemia
126977411 12697741 4 Type II hyperlipidaemia
126977411 12697741 5 Hypertension

Outcome of event

Event ID CASEID OUTC COD
126977411 12697741 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126977411 12697741 Myopathy
126977411 12697741 Pain

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

no results found

Therapies reported

no results found