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
125739581 12573958 1 I 20160611 20160708 20160720 20160720 EXP GB-MHRA-EYC 00141942 GB-TEVA-677199ACC TEVA 63.00 YR F Y 65.31000 KG 20160720 CN 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
125739581 12573958 1 PS GABAPENTIN. GABAPENTIN 1 Oral U 019411 76017 300 MG
125739581 12573958 2 C ADCAL-D3 CALCIUM CARBONATECHOLECALCIFEROL 1 0
125739581 12573958 3 C ASPIRIN. ASPIRIN 1 0
125739581 12573958 4 C COLESTYRAMIN 2 0
125739581 12573958 5 C FOLIC ACID. FOLIC ACID 1 0
125739581 12573958 6 C HYDROXYCHLOROQUINE HYDROXYCHLOROQUINE 1 0
125739581 12573958 7 C PREDNISOLONE. PREDNISOLONE 1 0
125739581 12573958 8 C SIMVASTATIN. SIMVASTATIN 1 0
125739581 12573958 9 C VALACICLOVIR VALACYCLOVIR HYDROCHLORIDE 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125739581 12573958 1 Neuralgia
125739581 12573958 4 Prophylaxis against diarrhoea

Outcome of event

Event ID CASEID OUTC COD
125739581 12573958 OT
125739581 12573958 DS

Reactions reported

Event ID CASEID DRUG REC ACT PT
125739581 12573958 Back pain
125739581 12573958 Diarrhoea
125739581 12573958 Malaise
125739581 12573958 Vision blurred

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
125739581 12573958 1 20160607 0