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
119974853 11997485 3 F 2015 20160926 20160203 20160927 EXP US-ABBVIE-16K-163-1550377-00 ABBVIE 0.00 F Y 71.28000 KG 20160927 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
119974853 11997485 1 PS HUMIRA ADALIMUMAB 1 Subcutaneous 1043237 125057 40 MG SOLUTION FOR INJECTION IN PRE-FILLED SYRINGE QOW
119974853 11997485 2 C FOLIC ACID. FOLIC ACID 1 0
119974853 11997485 3 C FUROSEMIDE. FUROSEMIDE 1 0
119974853 11997485 4 C TYLENOL ACETAMINOPHEN 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
119974853 11997485 1 Psoriasis
119974853 11997485 2 Product used for unknown indication
119974853 11997485 3 Peripheral swelling
119974853 11997485 4 Arthralgia

Outcome of event

Event ID CASEID OUTC COD
119974853 11997485 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
119974853 11997485 Peripheral swelling
119974853 11997485 Psoriasis
119974853 11997485 Renal failure

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
119974853 11997485 1 201505 0