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
125569701 12556970 1 I 20160620 20160701 20160714 20160714 PER US-TAKEDA-2016TUS011843 TAKEDA 45.43 YR F Y 97.52000 KG 20160714 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
125569701 12556970 1 PS CONTRAVE BUPROPION HYDROCHLORIDENALTREXONE HYDROCHLORIDE 1 Oral 8MG/90MG, QD Y UNKNOWN 200063 PROLONGED-RELEASE TABLET QD
125569701 12556970 2 SS IMODIUM LOPERAMIDE HYDROCHLORIDE 1 Unknown UNK U 0
125569701 12556970 3 C T3 LIOTHYRONINE SODIUM 1 Oral 25 ?G, QD U 0 25 UG QD
125569701 12556970 4 C ARMOUR THYROID THYROID, PORCINE 1 Oral 25 ?G, BID U 0 25 UG BID
125569701 12556970 5 C MINASTRIN 24 FE ETHINYL ESTRADIOLNORETHINDRONE ACETATE 1 Oral UNK, QD U 0 TABLET QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125569701 12556970 1 Weight control
125569701 12556970 2 Irritable bowel syndrome
125569701 12556970 3 Hypothyroidism
125569701 12556970 4 Hypothyroidism
125569701 12556970 5 Oral contraception

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
125569701 12556970 Abdominal pain
125569701 12556970 Cold sweat
125569701 12556970 Diarrhoea
125569701 12556970 Drug interaction
125569701 12556970 Malaise
125569701 12556970 Nausea
125569701 12556970 Somnolence
125569701 12556970 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
125569701 12556970 1 20160620 20160620 0
125569701 12556970 3 201604 0
125569701 12556970 4 201604 0