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
856301725 8563017 25 F 20120502 20160726 20120515 20160729 EXP CA-ROCHE-1066242 ROCHE 60.98 YR F Y 70.30000 KG 20160729 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
856301725 8563017 1 PS RITUXAN RITUXIMAB 1 Intravenous (not otherwise specified) DAY 1 AND DAY 15 N35021,B62272,B62422,H06573 103705 1000 MG SOLUTION FOR INFUSION
856301725 8563017 2 SS RITUXAN RITUXIMAB 1 Intravenous (not otherwise specified) N35021,B62272,B62422,H06573 103705 SOLUTION FOR INFUSION
856301725 8563017 3 SS ACETAMINOPHEN. ACETAMINOPHEN 1 Oral 0 650 MG QD
856301725 8563017 4 SS GRAVOL DIMENHYDRINATE 1 Unknown 0 100 MG QD
856301725 8563017 5 SS GRAVOL DIMENHYDRINATE 1 Unknown 0 50 MG
856301725 8563017 6 SS DIAMICRON GLICLAZIDE 1 Unknown 0
856301725 8563017 7 SS DIAMICRON GLICLAZIDE 1 0
856301725 8563017 8 SS LISINOPRIL. LISINOPRIL 1 Oral 0
856301725 8563017 9 SS ATACAND CANDESARTAN CILEXETIL 1 Unknown 0
856301725 8563017 10 SS NORVASC AMLODIPINE BESYLATE 1 Unknown 0
856301725 8563017 11 SS ALTACE RAMIPRIL 1 Unknown 0
856301725 8563017 12 SS SYNTHROID LEVOTHYROXINE SODIUM 1 Unknown 0
856301725 8563017 13 SS STEMETIL PROCHLORPERAZINE MALEATE 1 Unknown 0
856301725 8563017 14 SS MORPHINE MORPHINE 1 Unknown 0
856301725 8563017 15 SS MORPHINE MORPHINE 1 Unknown 0
856301725 8563017 16 SS NEXIUM ESOMEPRAZOLE MAGNESIUM 1 Unknown 0
856301725 8563017 17 SS DIPHENHYDRAMINE HYDROCHLORIDE. DIPHENHYDRAMINE HYDROCHLORIDE 1 Oral 0 50 MG QD
856301725 8563017 18 SS METHYLPREDNISOLONE. METHYLPREDNISOLONE 1 Intravenous (not otherwise specified) 0 100 MG QD
856301725 8563017 19 SS PREDNISONE. PREDNISONE 1 Unknown 0
856301725 8563017 20 C LANTUS INSULIN GLARGINE 1 0
856301725 8563017 21 C DOMPERIDONE DOMPERIDONE 1 0
856301725 8563017 22 C ELTROXIN LEVOTHYROXINE 1 0
856301725 8563017 23 C EZETROL EZETIMIBE 1 0
856301725 8563017 24 C CRESTOR ROSUVASTATIN CALCIUM 1 0
856301725 8563017 25 C LYRICA PREGABALIN 1 0
856301725 8563017 26 C DEPO-MEDROL METHYLPREDNISOLONE ACETATE 1 0
856301725 8563017 27 C JANUVIA SITAGLIPTIN PHOSPHATE 1 0
856301725 8563017 28 C APO-HYDRO HYDROCHLOROTHIAZIDE 1 Unknown 0
856301725 8563017 29 C TYLENOL ACETAMINOPHEN 1 Oral 0 650 MG
856301725 8563017 30 C LEVEMIR INSULIN DETEMIR 1 0
856301725 8563017 31 C HUMALOG INSULIN LISPRO 1 0
856301725 8563017 32 C PANTOLOC PANTOPRAZOLE SODIUM 1 0
856301725 8563017 33 C ZOFRAN ONDANSETRON HYDROCHLORIDE 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
856301725 8563017 1 Sjogren's syndrome
856301725 8563017 2 Rheumatoid arthritis
856301725 8563017 3 Premedication
856301725 8563017 4 Premedication
856301725 8563017 6 Diabetes mellitus
856301725 8563017 7 Blood pressure measurement
856301725 8563017 8 Hypertension
856301725 8563017 9 Hypertension
856301725 8563017 10 Product used for unknown indication
856301725 8563017 11 Hypertension
856301725 8563017 12 Product used for unknown indication
856301725 8563017 13 Vomiting
856301725 8563017 14 Product used for unknown indication
856301725 8563017 16 Product used for unknown indication
856301725 8563017 17 Premedication
856301725 8563017 18 Premedication
856301725 8563017 19 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
856301725 8563017 OT
856301725 8563017 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
856301725 8563017 Angina pectoris
856301725 8563017 Arterial occlusive disease
856301725 8563017 Arthritis
856301725 8563017 Asthenia
856301725 8563017 Blood pressure increased
856301725 8563017 Cataract
856301725 8563017 Chest discomfort
856301725 8563017 Fatigue
856301725 8563017 Gangrene
856301725 8563017 Gastric disorder
856301725 8563017 Headache
856301725 8563017 Nausea
856301725 8563017 Palpitations
856301725 8563017 Rheumatoid arthritis
856301725 8563017 Sinusitis

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
856301725 8563017 1 20070525 0
856301725 8563017 2 20130424 0
856301725 8563017 3 20120420 0
856301725 8563017 4 20120420 20120420 0
856301725 8563017 5 20130410 0
856301725 8563017 17 20111220 0
856301725 8563017 18 20120420 0
856301725 8563017 29 20130410 0