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
125002102 12500210 2 F 20160616 20160714 20160627 20160721 EXP JP-GLAXOSMITHKLINE-JP2016JPN089242 GLAXOSMITHKLINE 86.02 YR F Y 33.00000 KG 20160721 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
125002102 12500210 1 PS VALTREX VALACYCLOVIR HYDROCHLORIDE 1 Oral 3000 MG, 1D Y 20487 3000 MG TABLET QD
125002102 12500210 2 SS VALTREX VALACYCLOVIR HYDROCHLORIDE 1 Oral 500 MG, 1D Y 20487 500 MG TABLET QD
125002102 12500210 3 C CELECOX CELECOXIB 1 UNK 0
125002102 12500210 4 C LYRICA PREGABALIN 1 UNK 0
125002102 12500210 5 C UNKNOWN DRUG UNSPECIFIED INGREDIENT 1 UNK 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125002102 12500210 1 Herpes zoster
125002102 12500210 5 Angina pectoris

Outcome of event

Event ID CASEID OUTC COD
125002102 12500210 OT
125002102 12500210 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
125002102 12500210 Decreased appetite
125002102 12500210 Malaise
125002102 12500210 Renal impairment

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
125002102 12500210 1 20160614 0
125002102 12500210 2 20160616 20160616 0