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
125368921 12536892 1 I 20120924 20160629 20160707 20160707 EXP JP-SA-2016SA122090 AVENTIS 68.00 YR E M Y 74.00000 KG 20160707 CN JP JP

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
125368921 12536892 1 PS PLAVIX CLOPIDOGREL BISULFATE 1 Unknown Y UNK 20839 75 MG QD
125368921 12536892 2 SS PLAVIX CLOPIDOGREL BISULFATE 1 Unknown START DATE: BEING USED FROM BEFORE THE DAY OF CONSENT Y UNK 20839
125368921 12536892 3 C LOXONIN LOXOPROFEN SODIUM 1 0 TABLET
125368921 12536892 4 C LOXONIN LOXOPROFEN SODIUM 1 0 TABLET
125368921 12536892 5 C PLETAAL OD CILOSTAZOL 1 ONGOING AFTER END OF POST-TREATMENTOBSERVATION PERIOD 0 TABLET
125368921 12536892 6 C ADALAT CC NIFEDIPINE 1 0 TABLET
125368921 12536892 7 C SALOBEL ALLOPURINOL 1 0 TABLET
125368921 12536892 8 C LIPITOR ATORVASTATIN CALCIUM 1 0 TABLET

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125368921 12536892 1 Arteriosclerosis
125368921 12536892 2 Arteriosclerosis

Outcome of event

Event ID CASEID OUTC COD
125368921 12536892 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
125368921 12536892 Haematuria
125368921 12536892 Synovial cyst

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
125368921 12536892 1 20120221 20130628 0
125368921 12536892 2 20120220 0
125368921 12536892 3 20120207 20120209 0
125368921 12536892 4 20120926 20121002 0
125368921 12536892 5 20130709 0