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
125214061 12521406 1 I 20160615 20160617 20160701 20160701 EXP BR-SUN PHARMACEUTICAL INDUSTRIES LTD-2016R5-118996 RANBAXY 57.00 YR F Y 56.00000 KG 20160701 CN BR BR

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
125214061 12521406 1 PS VENLAFAXINE VENLAFAXINE HYDROCHLORIDE 1 Oral 75 MG, QD Y 2723953 78627 75 MG TABLET
125214061 12521406 2 C Taxofen 2 Oral 20 MG, QD U 0 20 MG

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125214061 12521406 1 Feeling hot
125214061 12521406 2 Breast cancer

Outcome of event

Event ID CASEID OUTC COD
125214061 12521406 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125214061 12521406 Abdominal pain
125214061 12521406 Abdominal pain upper
125214061 12521406 Dizziness
125214061 12521406 Dysgeusia
125214061 12521406 Feeling hot
125214061 12521406 Headache
125214061 12521406 Mental impairment
125214061 12521406 Nausea
125214061 12521406 Off label use
125214061 12521406 Peripheral swelling
125214061 12521406 Swollen tongue
125214061 12521406 Tachycardia
125214061 12521406 Tremor
125214061 12521406 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
125214061 12521406 1 20160615 20160615 0