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
125650591 12565059 1 I 20160407 20160513 20160718 20160718 EXP IT-AUROBINDO-AUR-APL-2016-06244 AUROBINDO 82.17 YR F Y 0.00000 20160718 OT IT IT

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
125650591 12565059 1 PS AMOXICILLIN. AMOXICILLIN 1 Oral 1000 MG, DAILY Y U 65256 1000 MG
125650591 12565059 2 C ONCO CARBIDE HYDROXYUREA 1 Oral 1 DF, UNK U 0 1 DF CAPSULE, HARD
125650591 12565059 3 C LOBIDIUR HYDROCHLOROTHIAZIDENEBIVOLOL HYDROCHLORIDE 1 Oral 1 DF, UNK U 0 1 DF FILM-COATED TABLET

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125650591 12565059 1 Product used for unknown indication
125650591 12565059 2 Thrombocytosis
125650591 12565059 3 Hypertension

Outcome of event

Event ID CASEID OUTC COD
125650591 12565059 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125650591 12565059 Presyncope
125650591 12565059 Pruritus
125650591 12565059 Rash generalised
125650591 12565059 Vomiting

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
125650591 12565059 1 20160407 20160407 0