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
126704491 12670449 1 I 20160817 20160822 20160822 EXP CA-AMGEN-CANSP2016108447 AMGEN 67.00 YR E F Y 0.00000 20160821 OT CA CA

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
126704491 12670449 1 PS ENBREL ETANERCEPT 1 Unknown UNK U 103795 UNKNOWN FORMULATION
126704491 12670449 2 SS CYMBALTA DULOXETINE HYDROCHLORIDE 1 Unknown UNK 0
126704491 12670449 3 SS METHOTREXATE SODIUM. METHOTREXATE SODIUM 1 Oral 20 MG, QWK 0 20 MG /wk
126704491 12670449 4 SS PLAQUENIL HYDROXYCHLOROQUINE SULFATE 1 Unknown UNK 0 TABLET
126704491 12670449 5 SS ZOSTAVAX VARICELLA-ZOSTER VIRUS STRAIN OKA/MERCK LIVE ANTIGEN 1 Unknown UNK 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126704491 12670449 1 Rheumatoid arthritis
126704491 12670449 2 Rheumatoid arthritis
126704491 12670449 3 Rheumatoid arthritis
126704491 12670449 4 Product used for unknown indication
126704491 12670449 5 Prophylaxis

Outcome of event

Event ID CASEID OUTC COD
126704491 12670449 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126704491 12670449 Abasia
126704491 12670449 Arthralgia
126704491 12670449 Drug ineffective
126704491 12670449 Fatigue
126704491 12670449 Feeling hot
126704491 12670449 Immunisation reaction
126704491 12670449 Ocular vascular disorder
126704491 12670449 Ophthalmic vein thrombosis
126704491 12670449 Pain
126704491 12670449 Pain in extremity
126704491 12670449 Pyrexia

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

no results found

Therapies reported

no results found