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
123157002 12315700 2 F 20160303 20160824 20160428 20160901 EXP FR-ANSM-NT20160469 FR-MYLANLABS-2016M1017462 MYLAN 0.00 Y 0.00000 20160901 OT FR FR

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
123157002 12315700 1 PS FONDAPARINUX FONDAPARINUX 1 Subcutaneous 2.5 MG, QD 45 MG Y 21345 2.5 MG INJECTION QD
123157002 12315700 2 SS PLAVIX CLOPIDOGREL BISULFATE 1 Oral 75 MG, QD Y 0 75 MG FILM-COATED TABLET QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
123157002 12315700 1 Thrombophlebitis
123157002 12315700 2 Acute coronary syndrome

Outcome of event

Event ID CASEID OUTC COD
123157002 12315700 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
123157002 12315700 Abdominal wall haematoma
123157002 12315700 Anaemia
123157002 12315700 Off label use

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
123157002 12315700 1 20160303 20160320 0
123157002 12315700 2 201103 20160326 0