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
126970341 12697034 1 I 20160816 20160830 20160830 EXP DE-LUPIN PHARMACEUTICALS INC.-E2B_00006036 LUPIN 0.00 F Y 4.20000 KG 20160830 DE DE

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
126970341 12697034 1 PS LEVETIRACETAM. LEVETIRACETAM 1 Transmammary UNKNOWN 78154 2000 MG BID
126970341 12697034 2 SS LEVETIRACETAM. LEVETIRACETAM 1 Transmammary UNKNOWN 78154 2250 MG BID
126970341 12697034 3 SS LAMICTAL LAMOTRIGINE 1 Transmammary UNKNOWN 0 50 MG BID

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126970341 12697034 1 Epilepsy
126970341 12697034 3 Epilepsy

Outcome of event

Event ID CASEID OUTC COD
126970341 12697034 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126970341 12697034 Dehydration
126970341 12697034 Exposure during breast feeding
126970341 12697034 Foetal exposure during pregnancy
126970341 12697034 Gastrooesophageal reflux disease
126970341 12697034 Selective eating disorder
126970341 12697034 Urinary tract infection

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

no results found

Therapies reported

no results found