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
106140452 10614045 2 F 201406 20160908 20141128 20160914 EXP FR-ABBVIE-14P-056-1312998-00 ABBVIE 80.00 YR F 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
106140452 10614045 1 PS DEPAKOTE DIVALPROEX SODIUM 1 Oral 18723 500 MG TABLET BID
106140452 10614045 2 SS PAROXETINE HYDROCHLORIDE. PAROXETINE HYDROCHLORIDE 1 Oral U UNKNOWN 0 20 MG QD
106140452 10614045 3 SS MODOPAR BENSERAZIDE HYDROCHLORIDELEVODOPA 1 Oral U UNKNOWN 0 500 MG QD
106140452 10614045 4 SS GALANTAMINE HYDROBROMIDE. GALANTAMINE HYDROBROMIDE 1 Oral UNKNOWN 0 8 MG QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
106140452 10614045 1 Product used for unknown indication
106140452 10614045 2 Product used for unknown indication
106140452 10614045 3 Product used for unknown indication
106140452 10614045 4 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
106140452 10614045 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
106140452 10614045 Constipation
106140452 10614045 Extrapyramidal disorder

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

no results found

Therapies reported

no results found