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
125242361 12524236 1 I 20160206 20160624 20160704 20160704 EXP GB-MHRA-ADR 23525185 GB-ACCORD-041995 ACCORD 71.00 YR M Y 83.91000 KG 20160704 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
125242361 12524236 1 PS SIMVASTATIN. SIMVASTATIN 1 Oral Y 78155 10 MG
125242361 12524236 2 SS PRAVASTATIN. PRAVASTATIN 1 Oral 1 Y 200750018 10 MG
125242361 12524236 3 SS ATORVASTATIN ATORVASTATIN 1 Oral Y 0 40 MG
125242361 12524236 4 C BENDROFLUMETHIAZIDE BENDROFLUMETHIAZIDE 1 Oral 0 2.5 MG QD
125242361 12524236 5 C FOLIC ACID. FOLIC ACID 1 0 5 MG /wk
125242361 12524236 6 C METHOTREXATE. METHOTREXATE 1 0 15 MG /wk

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125242361 12524236 1 Blood cholesterol increased
125242361 12524236 2 Blood cholesterol increased
125242361 12524236 3 Blood cholesterol increased

Outcome of event

Event ID CASEID OUTC COD
125242361 12524236 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125242361 12524236 Abdominal pain
125242361 12524236 Epistaxis
125242361 12524236 Flatulence
125242361 12524236 Gastrointestinal disorder
125242361 12524236 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
125242361 12524236 1 20160322 20160324 0
125242361 12524236 2 20160510 20160528 0
125242361 12524236 3 20160128 20160214 0