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
127431831 12743183 1 I 20160810 20160907 20160914 20160914 EXP FR-ABBVIE-16P-056-1727557-00 ABBVIE 48.00 YR M Y 0.00000 20160914 OT FR FR

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
127431831 12743183 1 PS DEPAKOTE DIVALPROEX SODIUM 1 Oral Y UNKNOWN 18723 1000 MG GASTRO-RESISTANT TABLET QD
127431831 12743183 2 SS DEPAKOTE DIVALPROEX SODIUM 1 Oral Y UNKNOWN 18723 GASTRO-RESISTANT TABLET
127431831 12743183 3 C COMBIVIR LAMIVUDINEIDOVUDINE 1 0
127431831 12743183 4 C VIRAMUNE NEVIRAPINE 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127431831 12743183 1 Epilepsy
127431831 12743183 3 Product used for unknown indication
127431831 12743183 4 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
127431831 12743183 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
127431831 12743183 Coma
127431831 12743183 Hypertonia
127431831 12743183 Mydriasis
127431831 12743183 Respiratory distress

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
127431831 12743183 2 20160810 20160810 0