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
125400081 12540008 1 I 20160618 20160706 20160708 20160708 EXP US-GLAXOSMITHKLINE-US2016GSK097103 GLAXOSMITHKLINE 70.62 YR F Y 79.40000 KG 20160708 CN US US

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
125400081 12540008 1 PS WELLBUTRIN BUPROPION HYDROCHLORIDE 1 Oral U 18644
125400081 12540008 2 SS AMPYRA DALFAMPRIDINE 1 Oral 10 MG, BID Y 0000079857 0 10 MG BID
125400081 12540008 3 C REBIF INTERFERON BETA-1A 1 UNK 0
125400081 12540008 4 C AMLODIPINE AMLODIPINE BESYLATE 1 UNK 0
125400081 12540008 5 C LEVOTHYROXINE. LEVOTHYROXINE 1 UNK 0
125400081 12540008 6 C PRAVASTATIN. PRAVASTATIN 1 UNK 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125400081 12540008 1 Product used for unknown indication
125400081 12540008 2 Asthenia

Outcome of event

Event ID CASEID OUTC COD
125400081 12540008 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125400081 12540008 Dizziness
125400081 12540008 Gait disturbance
125400081 12540008 Glaucoma

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
125400081 12540008 2 20160618 20160618 0
125400081 12540008 3 2002 0