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
106648075 10664807 5 F 20151030 20160727 20141219 20160731 EXP PHEH2014US024688 NOVARTIS 63.22 YR F Y 81.63000 KG 20160801 CN US US

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
106648075 10664807 1 PS GILENYA FINGOLIMOD HYDROCHLORIDE 1 Oral 0.5 MG, QD F0017 22527 .5 MG CAPSULE QD
106648075 10664807 2 C AMANTADINE HCL AMANTADINE HYDROCHLORIDE 1 Unknown U 0
106648075 10664807 3 C ATORVASTATIN ATORVASTATIN 1 Unknown U 0
106648075 10664807 4 C CLINDAMYCIN PHOSPHATE. CLINDAMYCIN PHOSPHATE 1 Unknown U 0
106648075 10664807 5 C FLUOXETINE FLUOXETINE HYDROCHLORIDE 1 Unknown U 0
106648075 10664807 6 C FORTEO TERIPARATIDE 1 Unknown U 0
106648075 10664807 7 C GABAPENTIN. GABAPENTIN 1 Unknown U 0
106648075 10664807 8 C IRON IRON 1 Unknown U 0
106648075 10664807 9 C LISINOPRIL. LISINOPRIL 1 Unknown U 0
106648075 10664807 10 C MEGARED OMEGA 3 KRILL OIL 2 Unknown U 0
106648075 10664807 11 C MURO 128 SODIUM CHLORIDE 1 Unknown U 0
106648075 10664807 12 C NIACINAMIDE NIACINAMIDE 1 Unknown U 0
106648075 10664807 13 C PROLIA DENOSUMAB 1 Unknown U 0
106648075 10664807 14 C SIMVASTATIN. SIMVASTATIN 1 Unknown U 0
106648075 10664807 15 C SYNTHROID LEVOTHYROXINE SODIUM 1 Unknown U 0
106648075 10664807 16 C VITAMIN D CHOLECALCIFEROL 1 Unknown U 0
106648075 10664807 17 C VITAMIN D2 ERGOCALCIFEROL 1 Unknown U 0
106648075 10664807 18 C VIVACTIL PROTRIPTYLINE HYDROCHLORIDE 1 Unknown U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
106648075 10664807 1 Multiple sclerosis
106648075 10664807 2 Product used for unknown indication
106648075 10664807 3 Product used for unknown indication
106648075 10664807 4 Product used for unknown indication
106648075 10664807 5 Product used for unknown indication
106648075 10664807 6 Product used for unknown indication
106648075 10664807 7 Product used for unknown indication
106648075 10664807 8 Product used for unknown indication
106648075 10664807 9 Product used for unknown indication
106648075 10664807 10 Product used for unknown indication
106648075 10664807 11 Product used for unknown indication
106648075 10664807 12 Product used for unknown indication
106648075 10664807 13 Product used for unknown indication
106648075 10664807 14 Product used for unknown indication
106648075 10664807 15 Product used for unknown indication
106648075 10664807 16 Product used for unknown indication
106648075 10664807 17 Product used for unknown indication
106648075 10664807 18 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
106648075 10664807 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
106648075 10664807 Anaemia
106648075 10664807 Ataxia
106648075 10664807 Body height decreased
106648075 10664807 Cervical spinal stenosis
106648075 10664807 Corneal dystrophy
106648075 10664807 Diarrhoea
106648075 10664807 Dyspareunia
106648075 10664807 Fatigue
106648075 10664807 Hypersomnia
106648075 10664807 Hypoacusis
106648075 10664807 Joint injury
106648075 10664807 Libido decreased
106648075 10664807 Memory impairment
106648075 10664807 Multiple sclerosis relapse
106648075 10664807 Osteoporosis
106648075 10664807 Panic attack
106648075 10664807 Sexual dysfunction
106648075 10664807 Skeletal injury
106648075 10664807 Speech disorder
106648075 10664807 Spinal osteoarthritis
106648075 10664807 Stress
106648075 10664807 Urinary hesitation
106648075 10664807 Vitamin B12 deficiency
106648075 10664807 Weight decreased
106648075 10664807 White blood cell count 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
106648075 10664807 1 20141125 0