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
118353728 11835372 8 F 20130714 20160812 20151215 20160816 EXP CA-ROCHE-1251218 ROCHE 53.09 YR F Y 70.37000 KG 20160816 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
118353728 11835372 1 PS RITUXAN RITUXIMAB 1 Intravenous (not otherwise specified) B62502,B012,H06573,H0657B013,H0762, 103705 1000 MG SOLUTION FOR INFUSION
118353728 11835372 2 SS RITUXAN RITUXIMAB 1 Intravenous (not otherwise specified) B62502,B012,H06573,H0657B013,H0762, 103705 SOLUTION FOR INFUSION
118353728 11835372 3 SS CYMBALTA DULOXETINE HYDROCHLORIDE 1 Unknown 0 60 MG
118353728 11835372 4 SS CYMBALTA DULOXETINE HYDROCHLORIDE 1 Unknown 0 90 MG
118353728 11835372 5 C RATIO-OXYCOCET ACETAMINOPHENOXYCODONE HYDROCHLORIDE 1 Unknown 0
118353728 11835372 6 C BENADRYL DIPHENHYDRAMINE HYDROCHLORIDE 1 Oral 0 50 MG
118353728 11835372 7 C SOLU-MEDROL METHYLPREDNISOLONE SODIUM SUCCINATE 1 Intravenous (not otherwise specified) 0 100 MG
118353728 11835372 8 C METHOTREXATE. METHOTREXATE 1 0
118353728 11835372 9 C FOLIC ACID. FOLIC ACID 1 0
118353728 11835372 10 C PREDNISONE. PREDNISONE 1 0
118353728 11835372 11 C ALEVE NAPROXEN SODIUM 1 Unknown AS REQUIRED 0
118353728 11835372 12 C TYLENOL ARTHRITIS PAIN ACETAMINOPHEN 1 Unknown AS REQUIRED 0
118353728 11835372 13 C LOSARTAN. LOSARTAN 1 Unknown 0 1 DF TABLET QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
118353728 11835372 1 Rheumatoid arthritis
118353728 11835372 3 Depression
118353728 11835372 6 Premedication
118353728 11835372 7 Premedication

Outcome of event

Event ID CASEID OUTC COD
118353728 11835372 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
118353728 11835372 Abdominal pain
118353728 11835372 Arthralgia
118353728 11835372 Blood pressure increased
118353728 11835372 Cold sweat
118353728 11835372 Cough
118353728 11835372 Depression
118353728 11835372 Hypertension
118353728 11835372 Infusion related reaction
118353728 11835372 Musculoskeletal stiffness
118353728 11835372 Oral herpes
118353728 11835372 Oropharyngeal pain
118353728 11835372 Pain
118353728 11835372 Skin warm
118353728 11835372 White blood cell count increased

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
118353728 11835372 1 20130711 0
118353728 11835372 2 20150203 0
118353728 11835372 3 201410 0
118353728 11835372 5 201410 0
118353728 11835372 6 20130711 0
118353728 11835372 7 20130711 0