The Safety Rates Drug Report

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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
126781751 12678175 1 I 201510 20160104 20160823 20160823 PER US-ENDO PHARMACEUTICALS INC.-2016-000207 ENDO 71.00 YR F Y 45.40000 KG 20160823 US 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
126781751 12678175 1 PS VENLAFAXINE HCL VENLAFAXINE HYDROCHLORIDE 1 Oral UNKNOWN 90027 25 MG TABLETS QD
126781751 12678175 2 SS VENLAFAXINE ER VENLAFAXINE HYDROCHLORIDE 1 Oral 0 CAPSULE
126781751 12678175 3 SS VENLAFAXINE ER VENLAFAXINE HYDROCHLORIDE 1 Oral 50 MG 0 CAPSULE
126781751 12678175 4 SS VENLAFAXINE ER VENLAFAXINE HYDROCHLORIDE 1 Oral 25 MG 0 CAPSULE
126781751 12678175 5 C NEXIUM ESOMEPRAZOLE MAGNESIUM 1 0
126781751 12678175 6 C LORAZEPAM. LORAZEPAM 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126781751 12678175 1 Depression
126781751 12678175 2 Depression
126781751 12678175 5 Gastrooesophageal reflux disease
126781751 12678175 6 Anxiety

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
126781751 12678175 Drug ineffective
126781751 12678175 Nausea
126781751 12678175 Paraesthesia

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
126781751 12678175 1 2014 0
126781751 12678175 2 201511 0