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
126066941 12606694 1 I 20160516 20160715 20160729 20160729 EXP IT-SUN PHARMACEUTICAL INDUSTRIES LTD-2016RR-121174 RANBAXY 43.66 YR F Y 0.00000 20160729 OT IT IT

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
126066941 12606694 1 PS CITALOPRAM CITALOPRAM HYDROBROMIDE 1 Oral 1 DOSAGE 600 MG TOTAL U U 77032 600 MG
126066941 12606694 2 SS EN DELORAZEPAM 1 Intramuscular 1 DOSAGE 1 DF TOTAL U U 0 1 DF
126066941 12606694 3 C STILNOX ZOLPIDEM TARTRATE 1 Oral U U 0
126066941 12606694 4 C EFFEXOR VENLAFAXINE HYDROCHLORIDE 1 Oral 150 MG U U 0 150 MG
126066941 12606694 5 C TAVOR (LORAZEPAM) LORAZEPAM 1 Oral U U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126066941 12606694 1 Drug abuse
126066941 12606694 2 Drug abuse
126066941 12606694 3 Product used for unknown indication
126066941 12606694 4 Product used for unknown indication
126066941 12606694 5 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
126066941 12606694 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
126066941 12606694 Drug abuse
126066941 12606694 Sopor
126066941 12606694 Toxicity to various agents
126066941 12606694 Vomiting

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
126066941 12606694 1 20160516 20160516 0
126066941 12606694 2 20160516 20160516 0