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
102370195 10237019 5 F 2012 20160802 20140613 20160808 EXP US-BAYER-2014-052609 BAYER 69.00 YR E M Y 0.00000 20160808 OT 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
102370195 10237019 1 PS NEXAVAR SORAFENIB 1 Oral UNK N 21923 FILM-COATED TABLET
102370195 10237019 2 SS NEXAVAR SORAFENIB 1 Oral 400 MG, BID N AH006CR 21923 400 MG FILM-COATED TABLET BID
102370195 10237019 3 SS NEXAVAR SORAFENIB 1 Oral 2 TABLETS DAILY N 21923 400 MG FILM-COATED TABLET
102370195 10237019 4 SS NEXAVAR SORAFENIB 1 1 TABLET TWICE A DAY TO ALTERNATE WITH 1 TABLET IN THE MORNING AND 2 TABLETS IN THE EVENING N AH00TPA 21923 FILM-COATED TABLET
102370195 10237019 5 SS NEXAVAR SORAFENIB 1 Oral 1 TABLET TWICE A DAY TO ALTERNATE WITH 1 TABLET IN THE MORNING AND 2 TABLETS IN THE EVENING N BXH4C75 21923 FILM-COATED TABLET
102370195 10237019 6 SS NEXAVAR SORAFENIB 1 Oral 1 TABLET TWICE A DAY TO ALTERNATE WITH 1 TABLET IN THE MORNING AND 2 TABLETS IN THE EVENING N BXH5XH3 21923 FILM-COATED TABLET
102370195 10237019 7 C WARFARIN WARFARIN 1 0
102370195 10237019 8 C FUROSEMIDE. FUROSEMIDE 1 0
102370195 10237019 9 C ESOMEPRAZOLE ESOMEPRAZOLE 1 0
102370195 10237019 10 C GLIMEPIRIDE. GLIMEPIRIDE 1 0
102370195 10237019 11 C TOPROL XL METOPROLOL SUCCINATE 1 0
102370195 10237019 12 C STROVITE 2 0
102370195 10237019 13 C CARTIA XT DILTIAZEM HYDROCHLORIDE 1 0
102370195 10237019 14 C HYDROXYCHLOROQUINE HYDROXYCHLOROQUINE 1 0
102370195 10237019 15 C POTASSIUM POTASSIUM 1 0
102370195 10237019 16 C ATORVASTATIN ATORVASTATIN 1 0
102370195 10237019 17 C KOMBIGLYZE XR METFORMIN HYDROCHLORIDESAXAGLIPTIN HYDROCHLORIDE 1 0
102370195 10237019 18 C DIOVAN VALSARTAN 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
102370195 10237019 1 Thyroid cancer
102370195 10237019 2 Thyroid cancer
102370195 10237019 3 Thyroid cancer
102370195 10237019 4 Thyroid cancer
102370195 10237019 5 Thyroid cancer
102370195 10237019 6 Thyroid cancer

Outcome of event

Event ID CASEID OUTC COD
102370195 10237019 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
102370195 10237019 Abasia
102370195 10237019 Acne
102370195 10237019 Alopecia
102370195 10237019 Blister
102370195 10237019 Burning sensation
102370195 10237019 Dry skin
102370195 10237019 Impaired healing
102370195 10237019 Off label use
102370195 10237019 Pain in extremity
102370195 10237019 Peripheral swelling
102370195 10237019 Skin fissures
102370195 10237019 Skin lesion

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
102370195 10237019 1 20120116 0
102370195 10237019 2 20120531 0
102370195 10237019 4 2012 0