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
113927634 11392763 4 F 201502 20160622 20150818 20160707 EXP US-APOTEX-2015AP011519 APOTEX 56.63 YR M Y 0.00000 20160707 CN GB 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
113927634 11392763 1 PS PAROXETINE HYDROCHLORIDE. PAROXETINE HYDROCHLORIDE 1 Oral 20 MG, UNK U U 0933665 20031 20 MG TABLET
113927634 11392763 2 SS LAMICTAL LAMOTRIGINE 1 Unknown 100 MG, UNK U U 0 100 MG PROLONGED-RELEASE TABLET

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
113927634 11392763 1 Product used for unknown indication
113927634 11392763 2 Seizure

Outcome of event

Event ID CASEID OUTC COD
113927634 11392763 HO
113927634 11392763 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
113927634 11392763 Abasia
113927634 11392763 Amnesia
113927634 11392763 Aphasia
113927634 11392763 Cerebrovascular accident
113927634 11392763 Coma
113927634 11392763 Drug intolerance
113927634 11392763 Fall
113927634 11392763 Hospitalisation
113927634 11392763 Seizure
113927634 11392763 Spinal column injury
113927634 11392763 Thrombosis
113927634 11392763 Urticaria

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
113927634 11392763 2 200506 0