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
127181611 12718161 1 I 20141031 20160902 20160906 20160906 EXP GB-MHRA-EYC 00144488 GB-009507513-1609GBR002059 MERCK 69.00 YR F Y 60.77000 KG 20160906 CN GB GB

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
127181611 12718161 1 PS EZETROL EZETIMIBE 1 Oral 10MG TO 40MG N U 21445 TABLET
127181611 12718161 2 SS PRAVASTATIN. PRAVASTATIN 1 Oral 10MG TO 40MG N U 0
127181611 12718161 3 SS ATORVASTATIN ATORVASTATIN 1 10 MG TO 40MG N U 0
127181611 12718161 4 SS CLOFIBRATE CLOFIBRATE 1 Oral 10MG TO 40MG N U 0
127181611 12718161 5 SS ROSUVASTATIN. ROSUVASTATIN 1 Oral UNK N U 0
127181611 12718161 6 C IBUPROFEN. IBUPROFEN 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127181611 12718161 1 Blood cholesterol increased
127181611 12718161 2 Blood cholesterol increased
127181611 12718161 3 Blood cholesterol increased
127181611 12718161 4 Blood cholesterol increased
127181611 12718161 5 Blood cholesterol increased

Outcome of event

Event ID CASEID OUTC COD
127181611 12718161 DS
127181611 12718161 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
127181611 12718161 Arthropathy
127181611 12718161 Pain

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

no results found

Therapies reported

Event ID CASEID DSG DRUG SEQ START DT END DT DUR DUR COD
127181611 12718161 1 20141019 20160819 0
127181611 12718161 2 20141019 20160819 0
127181611 12718161 3 20141019 20160819 0
127181611 12718161 4 20141019 20160819 0
127181611 12718161 5 19411019 20160819 0