The Safety Rates Drug Report

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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
4542796 5706792 I 4542796-4 20011217 20041223 20041231 EXP US-ABBOTT-04P-163-0284756-00 ABBOTT 38 YR F Y 20041230

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
4542796 1005547278 PS VALPROATE SODIUM 1 UNKNOWN UNKNOWN
4542796 1005547279 SS VALPROATE SODIUM 1 UNKNOWN
4542796 1005547280 SS CARBAMAZEPINE 1 UNKNOWN UNKNOWN
4542796 1005547281 C CARNITINE 2 UNKNOWN
4542796 1005547282 C L-THYROXINE 2 UNKNOWN

Indications of drugs used

Event ID DRUG SEQ INDI PT
4542796 1005547278 CONVULSION
4542796 1005547280 CONVULSION
4542796 1005547281 DRUG USE FOR UNKNOWN INDICATION
4542796 1005547282 HYPOTHYROIDISM

Outcome of event

Event ID OUTC COD
4542796 HO

Reactions reported

Event ID PT
4542796 ADRENAL INSUFFICIENCY
4542796 ANOREXIA
4542796 APLASIA PURE RED CELL
4542796 BONE MARROW DEPRESSION
4542796 CONVULSION
4542796 DEMENTIA
4542796 PANCYTOPENIA
4542796 THROMBOCYTOPENIA
4542796 WEIGHT DECREASED

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
4542796 1005547278 19890101
4542796 1005547279 20020401
4542796 1005547280 19840101 20011201 17 YR