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
126073141 12607314 1 I 20160701 20160726 20160729 20160729 EXP GB-MHRA-EYC 00142701 GB-PFIZER INC-2016362358 PFIZER 40.00 YR M Y 101.60000 KG 20160729 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
126073141 12607314 1 PS VENLAFAXINE HCL VENLAFAXINE HYDROCHLORIDE 1 Oral 75 MG, 2X/DAY 20699 75 MG BID
126073141 12607314 2 SS VENLAFAXINE HCL VENLAFAXINE HYDROCHLORIDE 1 Oral 75 MG, DAILY (ONE DAY TAKING 75MG) 20699 75 MG
126073141 12607314 3 C BACLOFEN. BACLOFEN 1 UNK 0
126073141 12607314 4 C BUTRANS BUPRENORPHINE 1 5 MG, UNK 0 5 MG
126073141 12607314 5 C BUTRANS BUPRENORPHINE 1 20 MG, UNK 0 20 MG
126073141 12607314 6 C CARBAMAZEPINE. CARBAMAZEPINE 1 UNK 0
126073141 12607314 7 C RAMIPRIL. RAMIPRIL 1 UNK 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126073141 12607314 1 Depression

Outcome of event

Event ID CASEID OUTC COD
126073141 12607314 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126073141 12607314 Dizziness
126073141 12607314 Headache
126073141 12607314 Lethargy
126073141 12607314 Nausea
126073141 12607314 Pain

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

no results found

Therapies reported

no results found