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
126363691 12636369 1 I 201507 20150813 20160809 20160809 PER US-ABBVIE-15P-163-1448103-00 ABBVIE 57.87 YR M Y 83.99000 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
126363691 12636369 1 PS DEPAKOTE ER DIVALPROEX SODIUM 1 Oral UNKNOWN 21168 TABLET
126363691 12636369 2 SS DEPAKOTE ER DIVALPROEX SODIUM 1 Unknown UNKNOWN 21168
126363691 12636369 3 C LISINOPRIL. LISINOPRIL 1 0
126363691 12636369 4 C CELEXA CITALOPRAM HYDROBROMIDE 1 0
126363691 12636369 5 C SIMVASTATIN. SIMVASTATIN 1 0
126363691 12636369 6 C LANTANOPROST LATANOPROST 1 0
126363691 12636369 7 C BRIMONDIDINE 2 0
126363691 12636369 8 C METFORMIN METFORMIN HYDROCHLORIDE 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126363691 12636369 1 Bipolar disorder
126363691 12636369 3 Hypertension
126363691 12636369 4 Depression
126363691 12636369 5 Blood cholesterol increased
126363691 12636369 6 Glaucoma
126363691 12636369 7 Glaucoma
126363691 12636369 8 Diabetes mellitus

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
126363691 12636369 Apathy
126363691 12636369 Blood pressure decreased
126363691 12636369 Somnolence

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
126363691 12636369 1 2006 201507 0