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
126203261 12620326 1 I 20160729 20160803 20160803 EXP PHHY2016VE106634 NOVARTIS 0.00 M Y 0.00000 20160804 CN VE VE

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
126203261 12620326 1 PS TEGRETOL CARBAMAZEPINE 1 Unknown 400 MG, QD 16608 400 MG QD
126203261 12620326 2 SS TEGRETOL CARBAMAZEPINE 1 Unknown 200 MG, QD (STRENGTH: 200 MG) 16608 200 MG QD
126203261 12620326 3 SS TOPIRAMATE. TOPIRAMATE 1 Unknown 200 MG, QD U 0 200 MG QD
126203261 12620326 4 C VALCOTE VALPROATE SODIUM 1 Unknown UNK UNK, QD U 0 QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126203261 12620326 1 Brain neoplasm
126203261 12620326 3 Brain neoplasm
126203261 12620326 4 Brain neoplasm

Outcome of event

Event ID CASEID OUTC COD
126203261 12620326 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126203261 12620326 Product use issue
126203261 12620326 Reduced facial expression
126203261 12620326 Seizure

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

no results found

Therapies reported

no results found