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
125377041 12537704 1 I 20160206 20160624 20160707 20160707 EXP GB-MHRA-EYC 00141277 GB-TEVA-672091ACC TEVA 71.00 YR M Y 83.91000 KG 20160707 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
125377041 12537704 1 PS ATORVASTATIN ATORVASTATIN 1 Oral Y U 78773 40 MG
125377041 12537704 2 SS PRAVASTATIN. PRAVASTATIN 1 Oral 1 Y U 76056 10 MG
125377041 12537704 3 SS SIMVASTATIN. SIMVASTATIN 1 Oral Y U 76052 10 MG
125377041 12537704 4 C BENDROFLUMETHIAZIDE BENDROFLUMETHIAZIDE 1 Oral 2.5 MILLIGRAM DAILY; 0 2.5 MG QD
125377041 12537704 5 C FOLIC ACID. FOLIC ACID 1 0 5 MG /wk
125377041 12537704 6 C METHOTREXATE. METHOTREXATE 1 0 15 MG /wk

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125377041 12537704 1 Blood cholesterol increased
125377041 12537704 2 Blood cholesterol increased
125377041 12537704 3 Blood cholesterol increased

Outcome of event

Event ID CASEID OUTC COD
125377041 12537704 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125377041 12537704 Abdominal pain
125377041 12537704 Epistaxis
125377041 12537704 Flatulence
125377041 12537704 Gastrointestinal disorder
125377041 12537704 Muscle spasms

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
125377041 12537704 1 20160128 20160214 0
125377041 12537704 2 20160510 20160528 0
125377041 12537704 3 20160322 20160324 0