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
125844901 12584490 1 I 20160408 20160722 20160722 EXP GB-ABBVIE-16P-167-1683671-00 ABBVIE 0.00 F Y 0.00000 20160722 CN GB GB

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
125844901 12584490 1 PS DEPAKOTE DIVALPROEX SODIUM 1 Unknown Y UNKNOWN 18723 500 MG TABLET BID
125844901 12584490 2 C RAMIPRIL. RAMIPRIL 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125844901 12584490 1 Bipolar disorder
125844901 12584490 2 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
125844901 12584490 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
125844901 12584490 Abdominal pain upper
125844901 12584490 Alopecia
125844901 12584490 Balance disorder
125844901 12584490 Gastric disorder
125844901 12584490 Headache
125844901 12584490 Loss of consciousness
125844901 12584490 Peripheral swelling

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
125844901 12584490 1 20120629 20160311 0