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
127867642 12786764 2 F 201609 20160916 20160927 20160927 PER PHEH2016US024418 NOVARTIS 46.00 YR F Y 66.67000 KG 20160927 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
127867642 12786764 1 PS TEGRETOL CARBAMAZEPINE 1 Unknown U 16608
127867642 12786764 2 SS FLUVOXAMINE FLUVOXAMINE 1 Oral 250 MG, QD 0 250 MG TABLET QD
127867642 12786764 3 SS FLUVOXAMINE FLUVOXAMINE 1 Oral 300 MG, QD 0 300 MG TABLET QD
127867642 12786764 4 SS KLONOPIN CLONAZEPAM 1 Unknown U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127867642 12786764 1 Seizure
127867642 12786764 2 Obsessive-compulsive disorder
127867642 12786764 4 Anxiety

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
127867642 12786764 Abdominal discomfort
127867642 12786764 Back pain
127867642 12786764 Gastritis
127867642 12786764 Hepatic enzyme increased
127867642 12786764 Nausea
127867642 12786764 Retching
127867642 12786764 Vomiting

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

no results found

Therapies reported

no results found