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
126957341 12695734 1 I 20160825 20160829 20160829 EXP IT-009507513-1608ITA014112 MERCK 66.00 YR F Y 79.00000 KG 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
126957341 12695734 1 PS SIMVASTATIN. SIMVASTATIN 1 Y U 19766 FILM-COATED TABLET
126957341 12695734 2 SS PRAVASTATIN. PRAVASTATIN 1 Y U 0
126957341 12695734 3 SS ATORVASTATIN ATORVASTATIN 1 Y U 0
126957341 12695734 4 SS ROSUVASTATIN CALCIUM. ROSUVASTATIN CALCIUM 1 Y U 0
126957341 12695734 5 C EZETROL 10 MG COMPRESSE EZETIMIBE 1 0 TABLET
126957341 12695734 6 C LOBIVON NEBIVOLOL HYDROCHLORIDE 1 0 TABLET
126957341 12695734 7 C EUTIROX LEVOTHYROXINE SODIUM 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126957341 12695734 1 Type II hyperlipidaemia
126957341 12695734 2 Type II hyperlipidaemia
126957341 12695734 3 Type II hyperlipidaemia
126957341 12695734 4 Type II hyperlipidaemia
126957341 12695734 5 Type II hyperlipidaemia
126957341 12695734 6 Hypertension
126957341 12695734 7 Autoimmune thyroiditis

Outcome of event

Event ID CASEID OUTC COD
126957341 12695734 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126957341 12695734 Myopathy
126957341 12695734 Pain

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

no results found

Therapies reported

no results found