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
127209752 12720975 2 F 201603 20160830 20160907 20160908 EXP FR-SA-2016SA086248 AVENTIS 87.00 YR E F Y 0.00000 20160908 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
127209752 12720975 1 PS LOVENOX ENOXAPARIN SODIUM 1 Subcutaneous Y UNKNOWN 20164 6000 IU INJECTION QD
127209752 12720975 2 SS ARIXTRA FONDAPARINUX SODIUM 1 Subcutaneous Y UNKNOWN 0 1 DF
127209752 12720975 3 C LASILIX FUROSEMIDE 1 Unknown 0
127209752 12720975 4 C DIFFU K POTASSIUM CHLORIDE 1 Unknown 0
127209752 12720975 5 C ZOLPIDEM ZOLPIDEMOLPIDEM TARTRATE 1 Unknown 0
127209752 12720975 6 C SEROPRAM CITALOPRAM HYDROBROMIDE 1 Unknown 0 TABLET

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127209752 12720975 1 Atrial fibrillation
127209752 12720975 2 Atrial fibrillation

Outcome of event

Event ID CASEID OUTC COD
127209752 12720975 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
127209752 12720975 Acute generalised exanthematous pustulosis

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
127209752 12720975 1 20160220 20160303 0
127209752 12720975 2 20160304 0