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
110108485 11010848 5 F 201206 20160915 20150410 20160922 EXP DK-DKMA-ADR 22920503 PHHY2015DK038403 NOVARTIS 37.00 YR M Y 0.00000 20160922 OT DK DK

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
110108485 11010848 1 PS TEGRETOL CARBAMAZEPINE 1 Oral UNK Y 16608
110108485 11010848 2 C PHENYTOIN. PHENYTOIN 1 Unknown U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
110108485 11010848 1 Trigeminal neuralgia
110108485 11010848 2 Seizure

Outcome of event

Event ID CASEID OUTC COD
110108485 11010848 HO
110108485 11010848 DS

Reactions reported

Event ID CASEID DRUG REC ACT PT
110108485 11010848 Alopecia totalis
110108485 11010848 Dermatitis exfoliative
110108485 11010848 Drug reaction with eosinophilia and systemic symptoms
110108485 11010848 Eczema
110108485 11010848 Fungal infection
110108485 11010848 Gastric ulcer
110108485 11010848 Pyrexia
110108485 11010848 Renal impairment
110108485 11010848 Urticaria

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
110108485 11010848 1 201205 201206 0