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 |