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
126764761 12676476 1 I 20160213 20160404 20160823 20160823 EXP CO-GLAXOSMITHKLINE-CO2016GSK048001 GLAXOSMITHKLINE 46.00 YR F Y 0.00000 20160823 CN CO CO

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
126764761 12676476 1 SS KEPPRA LEVETIRACETAM 1 500 MG, TID U 0 500 MG TID
126764761 12676476 2 PS LAMOTRIGINE. LAMOTRIGINE 1 100 MG, BID U 20241 100 MG BID
126764761 12676476 3 SS Revolade ELTROMBOPAG 1 Oral 50 MG, QD 0 50 MG TABLET QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126764761 12676476 1 Epilepsy
126764761 12676476 2 Epilepsy
126764761 12676476 3 Thrombocytopenic purpura

Outcome of event

Event ID CASEID OUTC COD
126764761 12676476 HO
126764761 12676476 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126764761 12676476 Asthenia
126764761 12676476 Dizziness
126764761 12676476 Fatigue
126764761 12676476 Rash generalised
126764761 12676476 Seizure
126764761 12676476 Skin discolouration
126764761 12676476 Treatment noncompliance
126764761 12676476 Vaginal haemorrhage

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
126764761 12676476 3 20150727 201511 0