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
127293331 12729333 1 I 20160818 20160901 20160909 20160909 EXP GB-MHRA-EYC 00144340 GB-MYLANLABS-2016M1037539 MYLAN 0.00 Y 0.00000 20160909 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
127293331 12729333 1 PS BISOPROLOL BISOPROLOL 1 Oral 2.5 MG, QD 2.5 MG 5 017007 011019 75831 2.5 MG QD
127293331 12729333 2 C GLUCOSAMINE + CHONDROITIN /01430901/ 2 UNK U 0
127293331 12729333 3 C COD LIVER OIL COD LIVER OIL 1 UNK U 0
127293331 12729333 4 C ECHINACEA /01323501/ ECHINACEA PURPUREA 1 UNK U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127293331 12729333 1 Blood pressure management

Outcome of event

Event ID CASEID OUTC COD
127293331 12729333 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
127293331 12729333 Headache
127293331 12729333 Hypoaesthesia
127293331 12729333 Malaise
127293331 12729333 Pain

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
127293331 12729333 1 20160817 0