The Safety Rates Drug Report

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Drug     Injury     Quarter    

Person who experienced the adverse event (patient)

Event ID CASE I F COD FOLL SEQ IMAGE EVENT DT MFR DT FDA DT REPT COD MFR NUM MFR SNDR AGE AGE COD GNDR COD E SUB WT WT COD REPT DT OCCP COD DEATH DT TO MFR CONFID REPORTER COUNTRY
5198746 6433232 F 5198746-3 20061221 20070104 EXP GSK25 GLAXOSMITHKLINE 20 YR F Y 20070104 CN IRELAND

Drug(s) used by person

Event ID DRUG SEQ ROLE COD DRUGNAME VAL VBM ROUTE DOSE VBM DECHAL RECHAL LOT NUM EXP DT NDA NUM
5198746 1008010721 PS PAROXETINE HCL 1 ORAL 20031
5198746 1008010722 SS ALPRAZOLAM 1 ORAL
5198746 1008010723 SS CHLORPROMAZINE 1 ORAL 009149
5198746 1008010724 SS PROCYCLIDINE HYDROCHLORIDE 2MG TAB 1 ORAL 009818
5198746 1008010725 SS BUSPIRONE HCL 1 ORAL

Indications of drugs used

Event ID DRUG SEQ INDI PT
5198746 1008010721 DRUG USE FOR UNKNOWN INDICATION
5198746 1008010722 DRUG USE FOR UNKNOWN INDICATION
5198746 1008010723 DRUG USE FOR UNKNOWN INDICATION
5198746 1008010724 DRUG USE FOR UNKNOWN INDICATION
5198746 1008010725 DRUG USE FOR UNKNOWN INDICATION

Outcome of event

Event ID OUTC COD
5198746 OT

Reactions reported

Event ID PT
5198746 INTENTIONAL OVERDOSE
5198746 MYDRIASIS
5198746 PUPIL FIXED
5198746 SOMNOLENCE

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

no results found

Therapies reported

no results found