The Safety Rates Drug Report

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Drug     Injury     Quarter    

Person who experienced the adverse event (patient)

Event ID CASE I F COD FOLL SEQ IMAGE EVENT DT MFR DT FDA DT REPT COD MFR NUM MFR SNDR AGE AGE COD GNDR COD E SUB WT WT COD REPT DT OCCP COD DEATH DT TO MFR CONFID REPORTER COUNTRY
6250367 6988891 F 6250367-7 20090408 20090622 20090630 EXP PHHY2009DE17026 NOVARTIS PHARMACEUTICALS CORP. 69 M Y 100 KG 20090630 OT GERMANY

Drug(s) used by person

Event ID DRUG SEQ ROLE COD DRUGNAME VAL VBM ROUTE DOSE VBM DECHAL RECHAL LOT NUM EXP DT NDA NUM
6250367 1011810930 PS CARBAMAZEPINE 1 ORAL 150 MG, TID 016608
6250367 1011810931 SS CARBAMAZEPINE 1 ORAL 200 MG, TID 016608
6250367 1011810932 SS CARBAMAZEPINE 1 ORAL 300MG PREDOSE 016608
6250367 1011810933 SS CARBAMAZEPINE 1 ORAL 525MG 016608
6250367 1011810934 SS CARBAMAZEPINE 1 ORAL 600MG 016608
6250367 1011810935 SS CARBAMAZEPINE 1 ORAL 800MG 016608
6250367 1011810936 C SIMVASTATIN 1 ORAL 20 MG
6250367 1011810937 C ASPIRIN 1 ORAL 100MG
6250367 1011810938 C CEFTRIAXONE 1
6250367 1011810939 C METAMIZOL 2
6250367 1011810940 C AMITRIPTYLINE 2

Indications of drugs used

Event ID DRUG SEQ INDI PT
6250367 1011810930 NEURALGIA
6250367 1011810936 HYPERCHOLESTEROLAEMIA
6250367 1011810937 SPINAL DISORDER
6250367 1011810938 INFECTION
6250367 1011810939 NEURALGIA

Outcome of event

Event ID OUTC COD
6250367 HO

Reactions reported

Event ID PT
6250367 DRUG RASH WITH EOSINOPHILIA AND SYSTEMIC SYMPTOMS
6250367 PYREXIA
6250367 RASH MACULO-PAPULAR
6250367 TRANSAMINASES INCREASED

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

no results found

Therapies reported

Event ID DRUG SEQ START DT END DT DUR DUR COD
6250367 1011810930 20090324 20090408 16 DAY
6250367 1011810931 20090408
6250367 1011810932 20090201
6250367 1011810935 20080301