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
125706961 12570696 1 I 20160624 20160711 20160719 20160719 EXP US-TEVA-677501USA TEVA 0.00 F Y 0.00000 20160719 CN US 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
125706961 12570696 1 PS AMOXICILLIN. AMOXICILLIN 1 Y 61926 500 MG CAPSULE

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125706961 12570696 1 Infection prophylaxis

Outcome of event

Event ID CASEID OUTC COD
125706961 12570696 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125706961 12570696 Abdominal pain upper
125706961 12570696 Acute kidney injury
125706961 12570696 Chromaturia
125706961 12570696 Confusional state
125706961 12570696 Crystal urine present
125706961 12570696 Dizziness
125706961 12570696 Fatigue
125706961 12570696 Hypersomnia
125706961 12570696 Pyrexia
125706961 12570696 Rash pruritic
125706961 12570696 Renal pain
125706961 12570696 Skin haemorrhage
125706961 12570696 Urine output decreased
125706961 12570696 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
125706961 12570696 1 20160620 0