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
126159431 12615943 1 I 20160701 20160726 20160802 20160802 EXP GB-MHRA-EYC 00142701 GB-MYLANLABS-2016M1030920 MYLAN 0.00 Y 0.00000 20160802 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
126159431 12615943 1 PS VENLAFAXINE VENLAFAXINE HYDROCHLORIDE 1 Oral 75 MG, BID (WITH PROGRESSIVE REDUCTION (I.E ONE DAY TAKING 75MG ) TO WITHDRAW FROM MEDICATION) 77166 75 MG BID
126159431 12615943 2 C BACLOFEN. BACLOFEN 1 UNK U 0
126159431 12615943 3 C BUTRANS BUPRENORPHINE 1 5 MG, UNK U 0 5 MG
126159431 12615943 4 C BUTRANS BUPRENORPHINE 1 U 0 20 MG
126159431 12615943 5 C CARBAMAZEPINE. CARBAMAZEPINE 1 UNK U 0
126159431 12615943 6 C RAMIPRIL. RAMIPRIL 1 UNK U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126159431 12615943 1 Depression

Outcome of event

Event ID CASEID OUTC COD
126159431 12615943 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126159431 12615943 Dizziness
126159431 12615943 Headache
126159431 12615943 Lethargy
126159431 12615943 Nausea
126159431 12615943 Pain

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

no results found

Therapies reported

no results found