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
124229282 12422928 2 F 2015 20160705 20160601 20160718 EXP US-CATALENT PHARMA SOLUTIONS-CAT-000009-2016 CATALENT PHARMA 72.00 YR M Y 0.00000 20160718 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
124229282 12422928 1 PS VALPROIC ACID. VALPROIC ACID 1 Oral 750 MG, EVERY NIGHT Y U 73229 750 MG CAPSULE
124229282 12422928 2 SS VALPROIC ACID. VALPROIC ACID 1 Y U 73229 CAPSULE
124229282 12422928 3 C ARICEPT DONEPEZIL HYDROCHLORIDE 1 Unknown UNK 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
124229282 12422928 1 Dementia Alzheimer's type
124229282 12422928 2 Anger
124229282 12422928 3 Dementia Alzheimer's type

Outcome of event

Event ID CASEID OUTC COD
124229282 12422928 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
124229282 12422928 Asthenia
124229282 12422928 Coordination abnormal
124229282 12422928 Gait disturbance
124229282 12422928 Insomnia
124229282 12422928 Product use issue
124229282 12422928 Tremor

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
124229282 12422928 1 2015 2016 0