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
4345056 5733787 I 4345056-X 20040402 20040420 EXP 001230 BARR LABORATORIES 26 YR F N 20040416 OT

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
4345056 1004809775 PS PLAN B 1 ORAL 0.75 MGQ12HR, ORAL D D 21045

Indications of drugs used

Event ID DRUG SEQ INDI PT
4345056 1004809775 POST COITAL CONTRACEPTION

Outcome of event

Event ID OUTC COD
4345056 OT

Reactions reported

Event ID PT
4345056 ABDOMINAL PAIN LOWER
4345056 COMPLICATIONS OF MATERNAL EXPOSURE TO THERAPEUTIC DRUGS
4345056 ECTOPIC PREGNANCY
4345056 PREGNANCY AFTER POST COITAL CONTRACEPTION
4345056 VAGINAL HAEMORRHAGE

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

Event ID RPSR COD
4345056 FGN
4345056 HP
4345056 LIT
4345056 OTH

Therapies reported

Event ID DRUG SEQ START DT END DT DUR DUR COD
4345056 1004809775 1 DAY