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
125934451 12593445 1 I 20160706 20160715 20160726 20160726 EXP GB-MHRA-TPP20695213C848998YC1467820160178 PHHY2016GB098104 SANDOZ 35.00 YR F Y 73.00000 KG 20160726 OT GB GB

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
125934451 12593445 1 PS AMOXICILLIN. AMOXICILLIN 1 Unknown U 64076
125934451 12593445 2 C AMITRIPTYLINE HYDROCHLORIDE. AMITRIPTYLINE HYDROCHLORIDE 1 Unknown 1 DF, QD, AT NIGHT 202.957993 DF U 0 1 DF QD
125934451 12593445 3 C ERYTHROMYCIN. ERYTHROMYCIN 1 Unknown 2 DF, QID 8 DF U 0 2 DF QID

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125934451 12593445 1 Product used for unknown indication
125934451 12593445 2 Product used for unknown indication
125934451 12593445 3 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
125934451 12593445 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125934451 12593445 Rash
125934451 12593445 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
125934451 12593445 1 20160706 0
125934451 12593445 2 20151216 0
125934451 12593445 3 20160706 0