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
125434471 12543447 1 I 2010 20151209 20160711 20160711 PER US-TEVA-617602USA TEVA 0.00 F Y 58.97000 KG 20160711 CN UG 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
125434471 12543447 1 PS VENLAFAXINE VENLAFAXINE HYDROCHLORIDE 1 Oral 75 MILLIGRAM DAILY; Y 76565 75 MG CAPSULE QD
125434471 12543447 2 SS VENLAFAXINE VENLAFAXINE HYDROCHLORIDE 1 Y 76565
125434471 12543447 3 C LIPITOR ATORVASTATIN CALCIUM 1 Oral 20 MILLIGRAM DAILY; 0 20 MG TABLET QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125434471 12543447 1 Anxiety
125434471 12543447 2 Depression
125434471 12543447 3 Blood cholesterol abnormal

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
125434471 12543447 Crying
125434471 12543447 Dizziness
125434471 12543447 Drug ineffective
125434471 12543447 Feeling jittery
125434471 12543447 Irritability

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
125434471 12543447 1 2010 2010 0