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
126018651 12601865 1 I 20160606 0 20160727 20160727 DIR 50.00 YR F N 113.00000 LBS 20160718 N CN US

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
126018651 12601865 1 PS BACTRIM DS SULFAMETHOXAZOLETRIMETHOPRIM 1 Oral 1/2 PILL TWICE DAILY BY MOUTH N D 0 .5 DF BID
126018651 12601865 3 C ASPIR-LOW ASPIRIN 1 0
126018651 12601865 5 C PRILOSEC OMEPRAZOLE MAGNESIUM 1 0
126018651 12601865 7 C VITAMIN D CHOLECALCIFEROL 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126018651 12601865 1 Urinary tract infection

Outcome of event

Event ID CASEID OUTC COD
126018651 12601865 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126018651 12601865 Contusion
126018651 12601865 Musculoskeletal stiffness
126018651 12601865 Oropharyngeal pain
126018651 12601865 Pain
126018651 12601865 Pyrexia
126018651 12601865 Rash papular
126018651 12601865 Skin exfoliation
126018651 12601865 Swelling

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
126018651 12601865 1 20160517 20160617 0