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
125248011 12524801 1 I 20160523 20160608 20160704 20160704 EXP PHHY2016IT080663 NOVARTIS 21.27 YR M Y 0.00000 20160704 OT IT IT

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
125248011 12524801 1 PS TEGRETOL CARBAMAZEPINE 1 Oral 800 MG, QD 12000 MG Y 20234 800 MG EXTENDED RELEASE TABLET QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125248011 12524801 1 Epilepsy

Outcome of event

Event ID CASEID OUTC COD
125248011 12524801 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
125248011 12524801 Blood lactate dehydrogenase increased
125248011 12524801 Blood pressure diastolic decreased
125248011 12524801 Cholestasis
125248011 12524801 Eosinophilia
125248011 12524801 Hepatitis
125248011 12524801 Hepatotoxicity
125248011 12524801 Leukopenia
125248011 12524801 Monocytosis
125248011 12524801 Neutropenia
125248011 12524801 Pyrexia
125248011 12524801 Rash
125248011 12524801 Thrombocytopenia
125248011 12524801 Toxicity to various agents
125248011 12524801 Vertigo

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
125248011 12524801 1 20160509 20160523 0