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
4334632 5713530 F 4334632-6 20030801 20030916 20040408 EXP PHRM2003FR02479 NOVARTIS PHARMACEUTICALS CORP. 20 YR M Y 63 KG 20040324 MD

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
4334632 1004769674 SS PROPOFAN 2 ORAL
4334632 1004769675 PS TEGRETOL 1 ORAL 600 MG/DAY
4334632 1004769676 SS DI-ANTALVIC 2 ORAL

Indications of drugs used

Event ID DRUG SEQ INDI PT
4334632 1004769674 LUMBAR PUNCTURE HEADACHE
4334632 1004769675 PARTIAL SEIZURES
4334632 1004769676 LUMBAR PUNCTURE HEADACHE

Outcome of event

Event ID OUTC COD
4334632 HO
4334632 OT

Reactions reported

Event ID PT
4334632 ANTICONVULSANT DRUG LEVEL INCREASED
4334632 ATAXIA
4334632 DIPLOPIA
4334632 DRUG INTERACTION
4334632 ENCEPHALITIS VIRAL
4334632 HEADACHE
4334632 INFECTION
4334632 INTRACRANIAL PRESSURE INCREASED
4334632 LUMBAR PUNCTURE HEADACHE
4334632 MENINGITIS VIRAL
4334632 NUCLEAR MAGNETIC RESONANCE IMAGING BRAIN ABNORMAL
4334632 OPTIC NERVE DISORDER
4334632 PAPILLOEDEMA
4334632 RETINAL OEDEMA
4334632 VISUAL ACUITY REDUCED

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

Event ID RPSR COD
4334632 HP

Therapies reported

Event ID DRUG SEQ START DT END DT DUR DUR COD
4334632 1004769674 20030804