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
116685804 11668580 4 F 20151018 20160719 20151027 20160725 EXP JP-GLAXOSMITHKLINE-JP2015JPN148996 GLAXOSMITHKLINE 85.14 YR M Y 58.00000 KG 20160725 CN 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
116685804 11668580 1 PS VALTREX VALACYCLOVIR HYDROCHLORIDE 1 Oral 1000 MG, TID 6000 MG Y 20487 1000 MG TABLET TID
116685804 11668580 2 SS LYRICA PREGABALIN 1 Oral Y 0
116685804 11668580 3 C VIDARABINE VIDARABINE 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
116685804 11668580 1 Herpes zoster

Outcome of event

Event ID CASEID OUTC COD
116685804 11668580 HO
116685804 11668580 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
116685804 11668580 Acute kidney injury
116685804 11668580 Altered state of consciousness
116685804 11668580 Blood creatinine increased
116685804 11668580 Drug level increased
116685804 11668580 Dyskinesia
116685804 11668580 Gait disturbance
116685804 11668580 Renal impairment
116685804 11668580 Toxic encephalopathy
116685804 11668580 Tremor

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
116685804 11668580 1 20151016 20151019 0