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
124398422 12439842 2 F 20160418 20160718 20160606 20160722 EXP FR-SA-2016SA105617 AVENTIS 87.00 YR E F Y 64.00000 KG 20160722 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
124398422 12439842 1 SS KARDEGIC ASPIRIN LYSINE 1 Oral N UNKNOWN 0 160 MG POWDER FOR ORAL SOLUTION QD
124398422 12439842 2 PS LOVENOX ENOXAPARIN SODIUM 1 Subcutaneous N UNKNOWN 20164 4000 IU SOLUTION FOR INJECTION QD
124398422 12439842 3 C BURINEX BUMETANIDE 1 Oral 5 MG STRENGTH 0 5 MG TABLET QD
124398422 12439842 4 C LEVOTHYROX LEVOTHYROXINE 1 Oral LEVOTHYROX 125 MCG TABLE 0 125 UG TABLET QD
124398422 12439842 5 C EBIXA MEMANTINE HYDROCHLORIDE 1 Oral EBIXA 10 MG TABLET 0 10 MG TABLET BID
124398422 12439842 6 C COVERSYL PERINDOPRIL 1 Oral COVERSYL 5 MG TABLET 0 5 MG TABLET QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
124398422 12439842 1 Prophylaxis
124398422 12439842 2 Prophylaxis

Outcome of event

Event ID CASEID OUTC COD
124398422 12439842 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
124398422 12439842 Haematoma
124398422 12439842 Oedema
124398422 12439842 Purpura

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
124398422 12439842 1 20160412 20160419 0
124398422 12439842 2 20160414 20160419 0
124398422 12439842 3 20160410 0
124398422 12439842 4 20160410 0
124398422 12439842 5 20160410 0
124398422 12439842 6 20160410 0