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
125491952 12549195 2 F 20160714 20160712 20160718 EXP PHHY2016CN093544 NOVARTIS 34.00 YR M Y 0.00000 20160719 CN CN CN

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
125491952 12549195 1 PS TEGRETOL CARBAMAZEPINE 1 Oral 2 DF, QD (1 TO 2 TABLETS EVERY EVENING) 16608 2 DF TABLET QD
125491952 12549195 2 SS CARBAMAZEPINE. CARBAMAZEPINE 1 Unknown UNK U 16608
125491952 12549195 3 SS ORYZANOL GAMMA ORYZANOL 1 Unknown UNK U 0
125491952 12549195 4 SS SODIUM BENZOATE SODIUM BENZOATE 1 Unknown UNK U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125491952 12549195 1 Epilepsy
125491952 12549195 2 Product used for unknown indication
125491952 12549195 3 Product used for unknown indication
125491952 12549195 4 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
125491952 12549195 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125491952 12549195 Dizziness
125491952 12549195 Drug dependence
125491952 12549195 Exposure via father
125491952 12549195 Panic disorder

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

no results found

Therapies reported

no results found