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
125051702 12505170 2 F 201606 20160712 20160628 20160719 EXP JP-GLAXOSMITHKLINE-JP2016JPN089214 GLAXOSMITHKLINE 89.52 YR F Y 31.00000 KG 20160719 MD JP JP

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
125051702 12505170 1 PS VALTREX VALACYCLOVIR HYDROCHLORIDE 1 Oral 1 G, BID 4 G Y 20487 1 G TABLET BID
125051702 12505170 2 SS LOXONIN LOXOPROFEN SODIUM 1 Oral 60 MG, TID Y 0 60 MG TID
125051702 12505170 3 C LYRICA PREGABALIN 1 25 MG, BID 0 25 MG BID

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125051702 12505170 1 Herpes zoster

Outcome of event

Event ID CASEID OUTC COD
125051702 12505170 HO
125051702 12505170 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125051702 12505170 Acute kidney injury
125051702 12505170 Depressed level of consciousness
125051702 12505170 Drug level increased
125051702 12505170 Renal impairment
125051702 12505170 Urine output decreased

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
125051702 12505170 1 20160620 20160622 0
125051702 12505170 2 20160620 0
125051702 12505170 3 20160620 0