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
126279201 12627920 1 I 20160701 20160726 20160807 20160807 EXP GB-MHRA-EYC 00142701 GB-TEVA-681062ACC TEVA 40.00 YR M Y 101.60000 KG 20160807 CN GB GB

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
126279201 12627920 1 PS VENLAFAXINE VENLAFAXINE HYDROCHLORIDE 1 Oral U 76690 75 MG BID
126279201 12627920 2 C BACLOFEN. BACLOFEN 1 0
126279201 12627920 3 C BUTRANS BUPRENORPHINE 1 0 5 MG TRANSDERMAL PATCH
126279201 12627920 4 C BUTRANS BUPRENORPHINE 1 0 20 MG
126279201 12627920 5 C CARBAMAZEPINE. CARBAMAZEPINE 1 0
126279201 12627920 6 C RAMIPRIL. RAMIPRIL 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126279201 12627920 1 Depression

Outcome of event

Event ID CASEID OUTC COD
126279201 12627920 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126279201 12627920 Dizziness
126279201 12627920 Headache
126279201 12627920 Lethargy
126279201 12627920 Nausea
126279201 12627920 Pain

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

no results found