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
952339415 9523394 15 F 20130128 20160824 20130913 20160831 EXP CA-ROCHE-1185966 ROCHE 56.10 YR F Y 72.60000 KG 20160831 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
952339415 9523394 1 PS RITUXAN RITUXIMAB 1 Intravenous (not otherwise specified) DAY 1 AND 15?LAST DOSE WAS RECEIVED ON 12-FEB-2013. B62332,B60962,H0762 103705 1000 MG SOLUTION FOR INFUSION
952339415 9523394 2 SS RITUXAN RITUXIMAB 1 Intravenous (not otherwise specified) DAY 1 AND 15 B62332,B60962,H0762 103705 1000 MG SOLUTION FOR INFUSION
952339415 9523394 3 SS RITUXAN RITUXIMAB 1 Intravenous (not otherwise specified) DAY 1 AND 15 B62332,B60962,H0762 103705 1000 MG SOLUTION FOR INFUSION
952339415 9523394 4 SS HERCEPTIN TRASTUZUMAB 1 Intravenous (not otherwise specified) U 103792 SOLUTION FOR INFUSION
952339415 9523394 5 SS NAPROXEN. NAPROXEN 1 Unknown 17581
952339415 9523394 6 SS KADCYLA ADO-TRASTUZUMAB EMTANSINE 1 Unknown 125427
952339415 9523394 7 C LEVOTHYROXINE. LEVOTHYROXINE 1 0
952339415 9523394 8 C CYMBALTA DULOXETINE HYDROCHLORIDE 1 0
952339415 9523394 9 C PREDNISONE. PREDNISONE 1 0
952339415 9523394 10 C PANTOLOC PANTOPRAZOLE SODIUM 1 0
952339415 9523394 11 C FOLIC ACID. FOLIC ACID 1 0
952339415 9523394 12 C LYSINE LYSINE 1 0
952339415 9523394 13 C NIACINAMIDE NIACINAMIDE 1 0
952339415 9523394 14 C VITAMIN E .ALPHA.-TOCOPHEROL 1 0
952339415 9523394 15 C PRIMROSE 2 0
952339415 9523394 16 C DIPHENHYDRAMINE HCL DIPHENHYDRAMINE HYDROCHLORIDE 1 Oral 0 50 MG
952339415 9523394 17 C ACETAMINOPHEN. ACETAMINOPHEN 1 Oral 0 650 MG
952339415 9523394 18 C METHYLPREDNISOLONE. METHYLPREDNISOLONE 1 Intravenous (not otherwise specified) 0 100 MG
952339415 9523394 19 C SYNTHROID LEVOTHYROXINE SODIUM 1 0
952339415 9523394 20 C ALOE VERA JUICE 2 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
952339415 9523394 1 Rheumatoid arthritis
952339415 9523394 4 Product used for unknown indication
952339415 9523394 5 Product used for unknown indication
952339415 9523394 6 Product used for unknown indication
952339415 9523394 16 Premedication
952339415 9523394 17 Premedication
952339415 9523394 18 Premedication

Outcome of event

Event ID CASEID OUTC COD
952339415 9523394 OT
952339415 9523394 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
952339415 9523394 Arthralgia
952339415 9523394 Asthenia
952339415 9523394 Breast cancer
952339415 9523394 Breast cancer metastatic
952339415 9523394 Breast cancer recurrent
952339415 9523394 Breast mass
952339415 9523394 Dehydration
952339415 9523394 Diarrhoea
952339415 9523394 Epistaxis
952339415 9523394 Fatigue
952339415 9523394 Gastrointestinal inflammation
952339415 9523394 Hypotension
952339415 9523394 Influenza
952339415 9523394 Infusion related reaction
952339415 9523394 Joint swelling
952339415 9523394 Nausea
952339415 9523394 Neuropathy peripheral
952339415 9523394 Osteoarthritis
952339415 9523394 Paranasal sinus discomfort
952339415 9523394 Throat irritation

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
952339415 9523394 1 20130128 20130212 0
952339415 9523394 2 20141218 0
952339415 9523394 3 20140619 0
952339415 9523394 6 20160823 0
952339415 9523394 16 20130128 0
952339415 9523394 17 20130128 0
952339415 9523394 18 20130128 0