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
5195438 6189342 F 5195438-1 20061030 20061207 20061230 EXP FR-ABBOTT-06P-056-0352697-00 ABBOTT 47 YR M Y 20061230 CN FRANCE

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
5195438 1007999424 PS DEPAKOTE 1 ORAL UNKNOWN 018723
5195438 1007999425 C MEPROBAMATE 1 ORAL
5195438 1007999426 C ACETAMINOPHEN 1 ORAL
5195438 1007999427 C MIRTAZAPINE 1 ORAL
5195438 1007999428 C BROMAZEPAM 2 ORAL
5195438 1007999429 C THIAMINE HCL 1 UNKNOWN

Indications of drugs used

Event ID DRUG SEQ INDI PT
5195438 1007999424 BIPOLAR DISORDER
5195438 1007999425 DRUG USE FOR UNKNOWN INDICATION
5195438 1007999426 DRUG USE FOR UNKNOWN INDICATION
5195438 1007999427 DRUG USE FOR UNKNOWN INDICATION
5195438 1007999428 DRUG USE FOR UNKNOWN INDICATION
5195438 1007999429 DRUG USE FOR UNKNOWN INDICATION

Outcome of event

Event ID OUTC COD
5195438 HO

Reactions reported

Event ID PT
5195438 DEHYDRATION
5195438 HYPERKALAEMIA
5195438 HYPONATRAEMIA
5195438 RENAL FAILURE ACUTE
5195438 RHABDOMYOLYSIS

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
5195438 1007999424 20061028 20061030
5195438 1007999425 20061022 20061023
5195438 1007999427 20061022 20061101
5195438 1007999428 20061022