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 CASE I F COD FOLL SEQ IMAGE EVENT DT MFR DT FDA DT REPT COD MFR NUM MFR SNDR AGE AGE COD GNDR COD E SUB WT WT COD REPT DT OCCP COD DEATH DT TO MFR CONFID REPORTER COUNTRY
5957530 6996336 I 5957530-0 20081028 20081112 EXP B0545198A GLAXOSMITHKLINE F N 20081110 MD INDIA

Drug(s) used by person

Event ID DRUG SEQ ROLE COD DRUGNAME VAL VBM ROUTE DOSE VBM DECHAL RECHAL LOT NUM EXP DT NDA NUM
5957530 1010720251 PS PROPRANOLOL HYDROCHLORIDE 1 TRANSPLACENTAL 30 MG, PER DAY, TRANSPLACENTARY Y D 21438
5957530 1010738808 SS CARBIMAZOLE 2 TRANSPLACENTAL 40 MG, PER DAY, TRANSPLACENTARY D D
5957530 1010738824 SS METHYLDOPA 1 TRANSPLACENTAL TRANSPLACENTARY D D

Indications of drugs used

no results found

Outcome of event

Event ID OUTC COD
5957530 CA
5957530 RI

Reactions reported

Event ID PT
5957530 CAESAREAN SECTION
5957530 CHOANAL ATRESIA
5957530 CYANOSIS
5957530 MATERNAL DRUGS AFFECTING FOETUS

Reporting Sources (this data is often not reported and may therefore be missing here)

Event ID RPSR COD
5957530 FGN
5957530 HP
5957530 LIT

Therapies reported

Event ID DRUG SEQ START DT END DT DUR DUR COD
5957530 1010738824 2 WK