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
127027111 12702711 1 I 20160803 20160808 20160831 20160831 EXP AU-PFIZER INC-2016383240 PFIZER 17.00 YR F Y 0.00000 20160831 OT AU AU

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
127027111 12702711 1 PS VANCOMYCIN HCL VANCOMYCIN HYDROCHLORIDE 1 2 G/ 24 HOUR Y 62911 2 G
127027111 12702711 2 SS VANCOMYCIN HCL VANCOMYCIN HYDROCHLORIDE 1 Y 62911
127027111 12702711 3 SS SODIUM CHLORIDE. SODIUM CHLORIDE 1 UNK Y 16366
127027111 12702711 4 C LYRICA PREGABALIN 1 Oral 150 MG, UNK 0 150 MG

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127027111 12702711 1 Infection
127027111 12702711 2 Spinal fusion surgery
127027111 12702711 4 Pain

Outcome of event

Event ID CASEID OUTC COD
127027111 12702711 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
127027111 12702711 Abdominal pain
127027111 12702711 Constipation
127027111 12702711 Pyrexia
127027111 12702711 Swelling face
127027111 12702711 Urticaria

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
127027111 12702711 1 20160716 20160816 0
127027111 12702711 3 20160716 20160806 0
127027111 12702711 4 20160701 0