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
127595201 12759520 1 I 20160724 20160905 20160919 20160919 EXP FR-PFIZER INC-2016418649 PFIZER 80.00 YR F Y 45.00000 KG 20160919 MD FR FR

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
127595201 12759520 1 PS SUNITINIB MALATE. SUNITINIB MALATE 1 Oral 50 MG, UNK Y N 21938 50 MG
127595201 12759520 2 C CO-APROVEL HYDROCHLOROTHIAZIDEIRBESARTAN 1 Oral 300 MG, DAILY 0 300 MG
127595201 12759520 3 C KEPPRA LEVETIRACETAM 1 Oral 250 MG, DAILY 0 250 MG
127595201 12759520 4 C OROCAL VITAMINE D3 /00278001/ 2 Oral 500 MG, DAILY 0 500 MG
127595201 12759520 5 C PARACETAMOL ACETAMINOPHEN 1 Oral 1000 MG, DAILY 0 1000 MG
127595201 12759520 6 C PARACETAMOL ACETAMINOPHEN 1 0
127595201 12759520 7 C PIZOTIFENE 2 Oral 0.5 MG, DAILY 0 .5 MG

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127595201 12759520 1 Metastatic renal cell carcinoma
127595201 12759520 2 Hypertension
127595201 12759520 3 Epilepsy
127595201 12759520 4 Osteoporosis
127595201 12759520 5 Pain
127595201 12759520 6 Prophylaxis
127595201 12759520 7 Headache

Outcome of event

Event ID CASEID OUTC COD
127595201 12759520 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
127595201 12759520 Diarrhoea
127595201 12759520 Escherichia urinary tract infection
127595201 12759520 Fatigue
127595201 12759520 Headache
127595201 12759520 Malaise
127595201 12759520 Vomiting

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
127595201 12759520 1 20160413 20160727 0
127595201 12759520 3 20160418 0