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
125388463 12538846 3 F 20160718 20160708 20160725 EXP US-UCBSA-2016008569 UCB 0.00 F Y 0.00000 20160725 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
125388463 12538846 1 PS LEVETIRACETAM. LEVETIRACETAM 1 UNK U 21035
125388463 12538846 2 SS VIMPAT LACOSAMIDE 1 50 MG, UNK U U 0 50 MG

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125388463 12538846 1 Product used for unknown indication
125388463 12538846 2 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
125388463 12538846 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125388463 12538846 Amnesia
125388463 12538846 Anger
125388463 12538846 Confusional state
125388463 12538846 Emotional disorder
125388463 12538846 Gastric disorder
125388463 12538846 Generalised tonic-clonic seizure
125388463 12538846 Headache
125388463 12538846 Mycobacterium avium complex infection
125388463 12538846 Pulmonary embolism
125388463 12538846 Seizure
125388463 12538846 Suicidal ideation
125388463 12538846 Thrombosis

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

no results found