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
125978712 12597871 2 F 20160624 20160822 20160727 20160829 PER US-PFIZER INC-2016358860 PFIZER 51.00 YR F Y 81.65000 KG 20160829 MD 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
125978712 12597871 1 PS VENLAFAXINE HCL VENLAFAXINE HYDROCHLORIDE 1 Oral 75 MG, 1X/DAY 375 MG Y 20699 75 MG PROLONGED-RELEASE CAPSULE QD
125978712 12597871 2 SS VENLAFAXINE HCL VENLAFAXINE HYDROCHLORIDE 1 375 MG Y 20699 PROLONGED-RELEASE CAPSULE
125978712 12597871 3 SS VENLAFAXINE HCL VENLAFAXINE HYDROCHLORIDE 1 375 MG Y 20699 PROLONGED-RELEASE CAPSULE

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125978712 12597871 1 Menopause
125978712 12597871 2 Depression
125978712 12597871 3 Panic attack

Outcome of event

Event ID CASEID OUTC COD
125978712 12597871 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125978712 12597871 Blood pressure increased
125978712 12597871 Feeling abnormal
125978712 12597871 Heart rate increased
125978712 12597871 Hypersensitivity
125978712 12597871 Lung disorder
125978712 12597871 Musculoskeletal pain
125978712 12597871 Myalgia
125978712 12597871 Nervousness
125978712 12597871 Pain
125978712 12597871 Product colour issue

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
125978712 12597871 1 20160620 20160624 0