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
950323610 9503236 10 F 20130218 20160712 20130906 20160714 EXP CA-ROCHE-1193288 ROCHE 52.52 YR F Y 69.40000 KG 20160714 CN 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
950323610 9503236 1 PS RITUXAN RITUXIMAB 1 Intravenous (not otherwise specified) LAST DOSE: 17/FEB/2015 B62282,B6239,B022 103705 1000 MG SOLUTION FOR INFUSION
950323610 9503236 2 SS RITUXAN RITUXIMAB 1 Intravenous (not otherwise specified) B62282,B6239,B022 103705 500 MG SOLUTION FOR INFUSION
950323610 9503236 3 SS RITUXAN RITUXIMAB 1 Intravenous (not otherwise specified) B62282,B6239,B022 103705 1000 MG SOLUTION FOR INFUSION
950323610 9503236 4 SS RITUXAN RITUXIMAB 1 Intravenous (not otherwise specified) B62282,B6239,B022 103705 1000 MG SOLUTION FOR INFUSION
950323610 9503236 5 SS RITUXAN RITUXIMAB 1 Intravenous (not otherwise specified) B62282,B6239,B022 103705 500 MG SOLUTION FOR INFUSION
950323610 9503236 6 SS NAPROSYN NAPROXEN 1 Oral U 17581 500 MG
950323610 9503236 7 SS NAPROSYN NAPROXEN 1 U 17581
950323610 9503236 8 SS AZITHROMYCIN ANHYDROUS. AZITHROMYCIN ANHYDROUS 1 Unknown Y 0
950323610 9503236 9 SS LEFLUNOMIDE. LEFLUNOMIDE 1 Unknown Y 0
950323610 9503236 10 C TYLENOL WITH CODEINE ACETAMINOPHENCODEINE PHOSPHATE 1 Oral 0 2 DF TABLET
950323610 9503236 11 C TYLENOL WITH CODEINE ACETAMINOPHENCODEINE PHOSPHATE 1 Unknown 0 1000 MG
950323610 9503236 12 C SYNTHROID LEVOTHYROXINE SODIUM 1 0
950323610 9503236 13 C OMEGA 3-6-9 (CANADA) 2 0
950323610 9503236 14 C DIPHENHYDRAMINE HCL DIPHENHYDRAMINE HYDROCHLORIDE 1 Oral 0 50 MG
950323610 9503236 15 C METHYLPREDNISOLONE. METHYLPREDNISOLONE 1 Intravenous (not otherwise specified) 0 100 MG
950323610 9503236 16 C ORENCIA ABATACEPT 1 Unknown 0
950323610 9503236 17 C PREDNISONE. PREDNISONE 1 Oral 0 5 MG QD
950323610 9503236 18 C PREDNISONE. PREDNISONE 1 0
950323610 9503236 19 C ACETAMINOPHEN. ACETAMINOPHEN 1 Oral 0 1000 MG
950323610 9503236 20 C ACETAMINOPHEN. ACETAMINOPHEN 1 Oral 0 650 MG
950323610 9503236 21 C REACTINE (CANADA) CETIRIZINE HYDROCHLORIDE 1 Intravenous (not otherwise specified) 0 10 MG
950323610 9503236 22 C MAXERAN METOCLOPRAMIDE HYDROCHLORIDE 1 Intravenous (not otherwise specified) 0 10 MG
950323610 9503236 23 C METOCLOPRAMIDE. METOCLOPRAMIDE 1 Intravenous (not otherwise specified) 0 10 MG
950323610 9503236 24 C CLARITIN (CANADA) 2 0
950323610 9503236 25 C FERROUS FUMARATE FERROUS FUMARATE 1 0
950323610 9503236 26 C RAMIPRIL. RAMIPRIL 1 0
950323610 9503236 27 C PANTOPRAZOLE PANTOPRAZOLE SODIUM 1 0
950323610 9503236 28 C ROSUVASTATIN. ROSUVASTATIN 1 0
950323610 9503236 29 C TICAGRELOR TICAGRELOR 1 0
950323610 9503236 30 C ACETYLSALICYLIC ACID ASPIRIN 1 Unknown 0 81 MG

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
950323610 9503236 1 Rheumatoid arthritis
950323610 9503236 2 Sjogren's syndrome
950323610 9503236 6 Sjogren's syndrome
950323610 9503236 7 Rheumatoid arthritis
950323610 9503236 8 Product used for unknown indication
950323610 9503236 9 Product used for unknown indication
950323610 9503236 10 Premedication
950323610 9503236 14 Premedication
950323610 9503236 15 Premedication
950323610 9503236 17 Sjogren's syndrome
950323610 9503236 18 Rheumatoid arthritis

Outcome of event

Event ID CASEID OUTC COD
950323610 9503236 OT
950323610 9503236 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
950323610 9503236 Alopecia
950323610 9503236 Cardiac disorder
950323610 9503236 Dizziness
950323610 9503236 Drug ineffective
950323610 9503236 Dyspnoea
950323610 9503236 Finger deformity
950323610 9503236 Hand deformity
950323610 9503236 Headache
950323610 9503236 Infarction
950323610 9503236 Infusion related reaction
950323610 9503236 Joint range of motion decreased
950323610 9503236 Lip swelling
950323610 9503236 Musculoskeletal stiffness
950323610 9503236 Nausea
950323610 9503236 Noninfective gingivitis
950323610 9503236 Pain
950323610 9503236 Paraesthesia
950323610 9503236 Product use issue
950323610 9503236 Psoriasis
950323610 9503236 Rash pruritic
950323610 9503236 Seasonal allergy
950323610 9503236 Synovitis
950323610 9503236 Tenderness
950323610 9503236 Tooth abscess
950323610 9503236 Vasculitis
950323610 9503236 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
950323610 9503236 1 20130218 0
950323610 9503236 2 20131010 0
950323610 9503236 3 20140620 0
950323610 9503236 4 20140606 0
950323610 9503236 5 20150203 0
950323610 9503236 8 2013 0
950323610 9503236 9 2013 0
950323610 9503236 10 20130218 20130218 0
950323610 9503236 14 20130218 0
950323610 9503236 15 20130218 0
950323610 9503236 16 20130814 0
950323610 9503236 19 20131010 0
950323610 9503236 20 20151104 0
950323610 9503236 21 20140620 0
950323610 9503236 22 20151104 0
950323610 9503236 23 20140620 0