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
126789051 12678905 1 I 20151214 20160811 20160824 20160824 EXP FR-UCBSA-2016031273 UCB 0.00 F Y 0.00000 20160824 OT FR FR

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
126789051 12678905 1 PS KEPPRA LEVETIRACETAM 1 1500 MG, 2X/DAY (BID) 21035 1500 MG BID
126789051 12678905 2 SS KEPPRA LEVETIRACETAM 1 UNKNOWN GRADUAL INCREASE 21035
126789051 12678905 3 SS KEPPRA LEVETIRACETAM 1 2500 MG IN THE MORNING AND 2000 MG IN THE EVENING, 2X/DAY (BID) 21035 BID

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126789051 12678905 1 Epilepsy

Outcome of event

Event ID CASEID OUTC COD
126789051 12678905 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126789051 12678905 Generalised tonic-clonic seizure
126789051 12678905 Head injury
126789051 12678905 Loss of consciousness
126789051 12678905 Pregnancy
126789051 12678905 Premature delivery
126789051 12678905 Seizure
126789051 12678905 Wound

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
126789051 12678905 2 2016 2016 0
126789051 12678905 3 2016 2016 0