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
126440071 12644007 1 I 20160521 20160803 20160811 20160811 EXP FR-PFIZER INC-2016373424 PFIZER 33.00 YR F Y 0.00000 20160811 OT FR FR

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
126440071 12644007 1 PS NEURONTIN GABAPENTIN 1 Oral 800 MG, 4X/DAY U 20882 800 MG FILM-COATED TABLET QID
126440071 12644007 2 SS DICODIN DIHYDROCODEINE 1 Oral 60 MG, 2X/DAY U 0 60 MG PROLONGED-RELEASE TABLET BID
126440071 12644007 3 C VENLAFAXINE VENLAFAXINE HYDROCHLORIDE 1 Oral 75 MG, 1X/DAY 0 75 MG PROLONGED-RELEASE CAPSULE QD
126440071 12644007 4 C LAROXYL AMITRIPTYLINE 1 Oral 25 MG, 1X/DAY 0 25 MG FILM-COATED TABLET QD

Indications of drugs used

no results found

Outcome of event

Event ID CASEID OUTC COD
126440071 12644007 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
126440071 12644007 Abdominal pain
126440071 12644007 Pancreatitis acute
126440071 12644007 Pyrexia

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
126440071 12644007 1 201512 0
126440071 12644007 2 20160309 0
126440071 12644007 3 20160324 0
126440071 12644007 4 20160309 0