The Safety Rates Drug Report

Member Login
2004.Q1    2004.Q2    2004.Q3    2004.Q4    2005.Q1    2005.Q2    2005.Q3    2005.Q4    2006.Q1    2006.Q2    2006.Q3    2006.Q4    2007.Q1    2007.Q2    2007.Q3    2007.Q4    2008.Q1    2008.Q2    2008.Q3    2008.Q4    2009.Q1    2009.Q2    2009.Q3    2009.Q4    2010.Q1    2010.Q2    2010.Q3    2010.Q4    2011.Q1    2011.Q2    2011.Q3    2011.Q4    2012.Q1    2012.Q2    2012.Q3    2012.Q4    2013.Q1    2013.Q2    2013.Q3    2013.Q4    2014.Q1    2014.Q2    2014.Q3    2014.Q4    2015.Q1    2015.Q2    2015.Q3    2015.Q4    2016.Q1    2016.Q2    2016.Q3   

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
109520115 10952011 5 F 20120118 20160912 20150325 20160915 EXP BR-ROCHE-1400690 ROCHE 46.21 YR F Y 57.00000 KG 20160915 OT BR BR

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
109520115 10952011 1 PS MABTHERA RITUXIMAB 1 Intravenous (not otherwise specified) DATE OF LATEST RITUXIMAB INFUSION: 16/FEB/2016 U 103705 SOLUTION FOR INFUSION
109520115 10952011 2 SS MABTHERA RITUXIMAB 1 Intravenous (not otherwise specified) U 103705 SOLUTION FOR INFUSION
109520115 10952011 3 SS MABTHERA RITUXIMAB 1 Intravenous (not otherwise specified) U 103705 SOLUTION FOR INFUSION
109520115 10952011 4 SS MABTHERA RITUXIMAB 1 Intravenous (not otherwise specified) U 103705 SOLUTION FOR INFUSION
109520115 10952011 5 SS MABTHERA RITUXIMAB 1 Intravenous (not otherwise specified) U 103705 SOLUTION FOR INFUSION
109520115 10952011 6 SS CIPRO CIPROFLOXACIN HYDROCHLORIDE 1 Unknown U 0
109520115 10952011 7 SS CORTISONE CORTISONEHYDROCORTISONE 1 Unknown U 0
109520115 10952011 8 SS ARADOIS LOSARTAN POTASSIUM 1 Unknown U 0
109520115 10952011 9 SS CONCOR BISOPROLOL FUMARATE 1 Unknown U 0
109520115 10952011 10 C CLOPIDOGREL BISULFATE. CLOPIDOGREL BISULFATE 1 Unknown 0 175 MG
109520115 10952011 11 C PRELONE PREDNISOLONE 1 Oral ALTERNATE DAYS 0 3 MG
109520115 10952011 12 C SYNTHROID LEVOTHYROXINE SODIUM 1 Unknown 0 75 MG
109520115 10952011 13 C PARIET RABEPRAZOLE SODIUM 1 Unknown 0 20 MG
109520115 10952011 14 C VYTORIN EZETIMIBESIMVASTATIN 1 Unknown 10/40 0
109520115 10952011 15 C MONTELAIR MONTELUKAST SODIUM 1 Unknown 0 10 MG
109520115 10952011 16 C ASPIRIN. ASPIRIN 1 Unknown 0 100 MG
109520115 10952011 17 C TRAYENTA DUO LINAGLIPTINMETFORMIN HYDROCHLORIDE 1 Unknown 0 25 MG
109520115 10952011 18 C DEPURA CHOLECALCIFEROL 1 0
109520115 10952011 19 C MACRODANTIN NITROFURANTOIN 1 0
109520115 10952011 20 C AZATHIOPRINE. AZATHIOPRINE 1 Unknown 0 150 MG
109520115 10952011 21 C RIVOTRIL CLONAZEPAM 1 Unknown 0 2 MG
109520115 10952011 22 C RIVOTRIL CLONAZEPAM 1 Unknown 0 1 MG
109520115 10952011 23 C PRISTIQ EXTENDED-RELEASE DESVENLAFAXINE SUCCINATE 1 0
109520115 10952011 24 C VASTAREL TRIMETAZIDINE DIHYDROCHLORIDE 1 0
109520115 10952011 25 C DIPYRONE DIPYRONE 1 0
109520115 10952011 26 C AZATHIOPRINE. AZATHIOPRINE 1 0
109520115 10952011 27 C PRELONE PREDNISOLONE 1 0
109520115 10952011 28 C CLOPINE CLOZAPINE 1 Unknown 0 75 MG
109520115 10952011 29 C ATORVASTATIN ATORVASTATIN 1 Unknown 0 20 MG
109520115 10952011 30 C EZETROL EZETIMIBE 1 Unknown 0 10 MG
109520115 10952011 31 C EZETROL EZETIMIBE 1 0
109520115 10952011 32 C SIGMATRIOL CALCITRIOL 1 Unknown 0 .25 MG
109520115 10952011 33 C VITAMIN D3 CHOLECALCIFEROL 1 0
109520115 10952011 34 C TRAMAL TRAMADOL 1 Unknown 0 50 MG
109520115 10952011 35 C ACETYLSALICYLIC ACID ASPIRIN 1 Unknown 0 100 MG

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
109520115 10952011 1 Rheumatoid arthritis
109520115 10952011 6 Product used for unknown indication
109520115 10952011 7 Product used for unknown indication
109520115 10952011 8 Product used for unknown indication
109520115 10952011 9 Product used for unknown indication
109520115 10952011 12 Thyroid disorder
109520115 10952011 15 Lung disorder
109520115 10952011 21 Pain
109520115 10952011 25 Pain
109520115 10952011 30 Blood cholesterol abnormal
109520115 10952011 31 Blood triglycerides abnormal

Outcome of event

Event ID CASEID OUTC COD
109520115 10952011 OT
109520115 10952011 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
109520115 10952011 Anaemia
109520115 10952011 Arterial occlusive disease
109520115 10952011 Arthralgia
109520115 10952011 Asthenia
109520115 10952011 Blood cholesterol increased
109520115 10952011 Blood glucose increased
109520115 10952011 Blood triglycerides increased
109520115 10952011 Cardiac failure congestive
109520115 10952011 Conjunctivitis
109520115 10952011 Depression
109520115 10952011 Disturbance in attention
109520115 10952011 Dizziness
109520115 10952011 Drug hypersensitivity
109520115 10952011 Dysbacteriosis
109520115 10952011 Dysstasia
109520115 10952011 Fall
109520115 10952011 Finger deformity
109520115 10952011 Fluid retention
109520115 10952011 Gait disturbance
109520115 10952011 Gastric haemorrhage
109520115 10952011 Glaucoma
109520115 10952011 Glucose tolerance impaired
109520115 10952011 H1N1 influenza
109520115 10952011 Haemorrhage
109520115 10952011 Hepatitis
109520115 10952011 Hypersensitivity
109520115 10952011 Hypertension
109520115 10952011 Hypotension
109520115 10952011 Hypothermia
109520115 10952011 Immunodeficiency
109520115 10952011 Influenza
109520115 10952011 Laryngeal oedema
109520115 10952011 Memory impairment
109520115 10952011 Mouth injury
109520115 10952011 Movement disorder
109520115 10952011 Muscle tightness
109520115 10952011 Muscular weakness
109520115 10952011 Myalgia
109520115 10952011 Myocardial infarction
109520115 10952011 Neck pain
109520115 10952011 Nephrocalcinosis
109520115 10952011 Nephrolithiasis
109520115 10952011 Oesophageal candidiasis
109520115 10952011 Pain
109520115 10952011 Pyelonephritis
109520115 10952011 Pyrexia
109520115 10952011 Skin papilloma
109520115 10952011 Somnolence
109520115 10952011 Unevaluable event
109520115 10952011 Urinary tract infection
109520115 10952011 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
109520115 10952011 1 20120103 0
109520115 10952011 2 201207 0
109520115 10952011 3 20130201 0
109520115 10952011 4 201405 0
109520115 10952011 5 201410 0