The Safety Rates Drug Report

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Drug     Injury     Quarter    

Person who experienced the adverse event (patient)

Event ID CASEID CASEVERSION I F COD EVENT DT MFR DT INIT FDA DT FDA DT REPT COD AUTH NUM MFR NUM MFR SNDR LIT REF AGE AGE COD AGE GRP GNDR COD E SUB WT WT COD REPT DT TO MFR OCCP COD REPORTER COUNTRY OCCR COUNTRY
126363021 12636302 1 I 20160217 20160809 20160809 PER US-ABBVIE-16P-163-1563403-00 ABBVIE 0.00 M Y 95.34000 KG 20160809 CN US US

Drug(s) used by person

Event ID CASEID DRUG SEQ ROLE COD DRUGNAME PROD AI VAL VBM ROUTE DOSE VBM CUM DOSE CHR CUM DOSE UNIT DECHAL RECHAL LOT NUM EXP DT NDA NUM DOSE AMT DOSE UNIT DOSE FORM DOSE FREQ
126363021 12636302 1 PS DEPAKOTE ER DIVALPROEX SODIUM 1 Oral Y UNKNOWN 21168 500 MG TID
126363021 12636302 2 SS DEPAKOTE ER DIVALPROEX SODIUM 1 Y UNKNOWN 21168
126363021 12636302 3 C RISPERIDONE. RISPERIDONE 1 OCCASIONAL USE 0
126363021 12636302 4 C SEROQUEL QUETIAPINE FUMARATE 1 0
126363021 12636302 5 C EFFEXOR VENLAFAXINE HYDROCHLORIDE 1 0
126363021 12636302 6 C WELLBUTRIN BUPROPION HYDROCHLORIDE 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126363021 12636302 1 Psychotic disorder
126363021 12636302 2 Bipolar disorder
126363021 12636302 3 Product used for unknown indication
126363021 12636302 4 Product used for unknown indication
126363021 12636302 5 Product used for unknown indication
126363021 12636302 6 Product used for unknown indication

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
126363021 12636302 Abdominal pain
126363021 12636302 Dyspnoea
126363021 12636302 Gait disturbance
126363021 12636302 Nausea
126363021 12636302 Overdose

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

no results found

Therapies reported

Event ID CASEID DSG DRUG SEQ START DT END DT DUR DUR COD
126363021 12636302 1 2005 2013 0