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
126652721 12665272 1 I 201508 20160808 20160818 20160818 EXP US-ABBVIE-16K-163-1698923-00 ABBVIE 54.02 YR M Y 70.37000 KG 20160818 CN COUNTRY NOT SPECIFIED US

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
126652721 12665272 1 PS HUMIRA ADALIMUMAB 1 Subcutaneous Y 1057214 125057 40 MG SOLUTION FOR INJECTION IN PRE-FILLED PEN QOW
126652721 12665272 2 SS HUMIRA ADALIMUMAB 1 Subcutaneous Y 1057214 125057 40 MG SOLUTION FOR INJECTION IN PRE-FILLED PEN /wk
126652721 12665272 3 SS MELOXICAM. MELOXICAM 1 Oral Y UNKNOWN 0 15 MG QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126652721 12665272 1 Rheumatoid arthritis
126652721 12665272 3 Rheumatoid arthritis

Outcome of event

Event ID CASEID OUTC COD
126652721 12665272 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126652721 12665272 Angiopathy
126652721 12665272 Dizziness
126652721 12665272 Drug ineffective
126652721 12665272 Flatulence
126652721 12665272 Gastrointestinal disorder
126652721 12665272 Injection site reaction
126652721 12665272 Lip swelling
126652721 12665272 Nausea
126652721 12665272 Toxicity to various agents

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
126652721 12665272 1 201502 201508 0
126652721 12665272 2 201508 20160621 0
126652721 12665272 3 20160521 20160721 0