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
125449016 12544901 6 F 20160529 20160927 20160711 20160930 EXP JP-GLAXOSMITHKLINE-JP2016JPN096498 GLAXOSMITHKLINE 49.18 YR F Y 50.00000 KG 20160930 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
125449016 12544901 1 PS VALTREX VALACYCLOVIR HYDROCHLORIDE 1 Oral 500 MG, BID 20487 TABLET
125449016 12544901 2 SS VALTREX VALACYCLOVIR HYDROCHLORIDE 1 20487 TABLET
125449016 12544901 3 SS TALION (JAPAN) BEPOTASTINE 1 Oral UNK 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125449016 12544901 1 Antiviral prophylaxis
125449016 12544901 2 Kaposi's varicelliform eruption
125449016 12544901 3 Dermatitis atopic

Outcome of event

Event ID CASEID OUTC COD
125449016 12544901 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125449016 12544901 Incorrect drug administration duration
125449016 12544901 Interstitial lung disease
125449016 12544901 Pulmonary fibrosis
125449016 12544901 Treatment noncompliance

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
125449016 12544901 1 20080624 0