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
121062343 12106234 3 F 201501 20160713 20160223 20160721 EXP BR-ABBVIE-16K-020-1552677-00 ABBVIE 62.44 YR F Y 100.00000 KG 20160721 CN COUNTRY NOT SPECIFIED BR

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
121062343 12106234 1 PS HUMIRA ADALIMUMAB 1 Subcutaneous UNKNOWN 125057 40 MG SOLUTION FOR INJECTION IN PRE-FILLED SYRINGE
121062343 12106234 2 SS HUMIRA ADALIMUMAB 1 Subcutaneous UNKNOWN 125057 40 MG SOLUTION FOR INJECTION IN PRE-FILLED SYRINGE
121062343 12106234 3 C AMYTRIL AMITRIPTYLINE HYDROCHLORIDE 1 Oral 1 OR 2 TABLETS DAILY 0 TABLET
121062343 12106234 4 C METHOTREXATE. METHOTREXATE 1 0 25 MG INJECTION /wk

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
121062343 12106234 1 Psoriatic arthropathy
121062343 12106234 3 Sleep disorder therapy
121062343 12106234 4 Psoriatic arthropathy

Outcome of event

Event ID CASEID OUTC COD
121062343 12106234 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
121062343 12106234 Arthropathy
121062343 12106234 Cough
121062343 12106234 Limb injury
121062343 12106234 Pain
121062343 12106234 Peripheral swelling
121062343 12106234 Psoriasis
121062343 12106234 Varicose vein
121062343 12106234 Varicose vein ruptured
121062343 12106234 Weight decreased

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
121062343 12106234 1 20110101 201507 0
121062343 12106234 3 2006 0
121062343 12106234 4 201510 0