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
124548862 12454886 2 F 201605 20160905 20160610 20160908 EXP FR-GLAXOSMITHKLINE-FR2016GSK081925 GLAXOSMITHKLINE 18.00 YR M Y 0.00000 20160908 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
124548862 12454886 1 PS LAMICTAL LAMOTRIGINE 1 Oral UNK Y 20241
124548862 12454886 2 C PARKINANE TRIHEXYPHENIDYL HYDROCHLORIDE 1 5 MG, UNK U 0 5 MG
124548862 12454886 3 C XEPLION PALIPERIDONE PALMITATE 1 75 MG, UNK U 0 75 MG

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
124548862 12454886 1 Depression

Outcome of event

Event ID CASEID OUTC COD
124548862 12454886 HO
124548862 12454886 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
124548862 12454886 Drug reaction with eosinophilia and systemic symptoms
124548862 12454886 Erythema
124548862 12454886 General physical health deterioration
124548862 12454886 Hepatitis
124548862 12454886 Hepatocellular injury
124548862 12454886 Malaise
124548862 12454886 Pyrexia

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
124548862 12454886 1 20160330 20160507 0