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
127230771 12723077 1 I 20160408 20160902 20160908 20160908 EXP JP-UCBSA-2016034244 UCB 81.65 YR M Y 0.00000 20160908 MD 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
127230771 12723077 1 PS LEVETIRACETAM. LEVETIRACETAM 1 Intravenous drip 500 MG, 2X/DAY (BID) 4000 MG U 21035 500 MG BID
127230771 12723077 2 SS E Keppra LEVETIRACETAM 1 500 MG, 2X/DAY (BID) U 21035 500 MG BID
127230771 12723077 3 C CEFTRIAXONE SODIUM. CEFTRIAXONE SODIUM 1 2 G, ONCE DAILY (QD) 10 G U 0 2 G QD
127230771 12723077 4 C DECADRON DEXAMETHASONE 1 1.65 MG, ONCE DAILY (QD) 8.25 MG U 0 1.65 MG QD
127230771 12723077 5 C Omepral OMEPRAZOLE 1 20 MG, ONCE DAILY (QD) 100 MG U 0 20 MG QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127230771 12723077 1 Complex partial seizures
127230771 12723077 2 Complex partial seizures
127230771 12723077 3 Product used for unknown indication
127230771 12723077 4 Product used for unknown indication
127230771 12723077 5 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
127230771 12723077 DE

Reactions reported

Event ID CASEID DRUG REC ACT PT
127230771 12723077 Death

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
127230771 12723077 1 20160404 20160407 0
127230771 12723077 2 20151229 201604 0
127230771 12723077 3 20160404 20160408 0
127230771 12723077 4 20160404 20160408 0
127230771 12723077 5 20160404 20160408 0