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
127066801 12706680 1 I 20160830 20160901 20160901 EXP IT-009507513-1608USA015807 MERCK 81.00 YR F Y 70.00000 KG 20160901 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
127066801 12706680 1 PS SIMVASTATIN. SIMVASTATIN 1 REDUCING THE DOSE Y U 19766 TABLET
127066801 12706680 2 SS PRAVASTATIN. PRAVASTATIN 1 REDUCING THE DOSE Y U 0
127066801 12706680 3 SS ATORVASTATIN ATORVASTATIN 1 REDUCING THE DOSE Y U 0
127066801 12706680 4 SS ROSUVASTATIN CALCIUM. ROSUVASTATIN CALCIUM 1 REDUCING THE DOSE Y U 0
127066801 12706680 5 C LOPRESSOR METOPROLOL TARTRATE 1 0
127066801 12706680 6 C TIKLID TICLOPIDINE HYDROCHLORIDE 1 0
127066801 12706680 7 C ZETIA EZETIMIBE 1 0 TABLET
127066801 12706680 8 C DIETARY SUPPLEMENT (UNSPECIFIED) DIETARY SUPPLEMENT 1 0
127066801 12706680 9 C OLPREZIDE HYDROCHLOROTHIAZIDEOLMESARTAN MEDOXOMIL 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127066801 12706680 5 Myocardial infarction
127066801 12706680 6 Myocardial infarction
127066801 12706680 7 Myocardial infarction
127066801 12706680 9 Myocardial infarction

Outcome of event

Event ID CASEID OUTC COD
127066801 12706680 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
127066801 12706680 Myopathy
127066801 12706680 Pain

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

no results found

Therapies reported

no results found