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
125203971 12520397 1 I 20120612 20151224 20160701 20160701 PER GB-MHRA-EYC 00120331 GB-LUPIN PHARMACEUTICALS INC.-E2B_00004718 LUPIN 64.00 YR M Y 96.16000 KG 20160701 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
125203971 12520397 1 PS SIMVASTATIN. SIMVASTATIN 1 Oral 80 MG Y U UNKNOWN 78103
125203971 12520397 2 C ASPIRIN. ASPIRIN 1 Unknown 0 75 MG QD
125203971 12520397 3 C OMEPRAZOLE. OMEPRAZOLE 1 Unknown 20 MG 0
125203971 12520397 4 C VIAGRA SILDENAFIL CITRATE 1 Unknown 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125203971 12520397 1 Blood cholesterol increased
125203971 12520397 2 Product used for unknown indication
125203971 12520397 3 Dyspepsia
125203971 12520397 4 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
125203971 12520397 DS

Reactions reported

Event ID CASEID DRUG REC ACT PT
125203971 12520397 Arthralgia
125203971 12520397 Mobility decreased
125203971 12520397 Myalgia
125203971 12520397 Pain in extremity
125203971 12520397 Tenderness

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
125203971 12520397 1 20120609 201501 0
125203971 12520397 3 2012 0
125203971 12520397 4 2012 0