Non Serious Adverse Drug Reactions Report

Start Date:2016-06-08 End Date:2016-06-09
Study :EMR700623-541Investigator :Ying ZhongCountry of Investigator :ChinaSiteNo:C05
Subject No :C05-0117Subject Initials :Y-LDOB :04/16/1982Sex:FemaleRace:AsianHeight:165cmWeight:48kg
First administration date of batch :Batch number :
Study DrugStart DateDoseChange in Dose
Gonal-f New Pen Stimulation Treatment08/23/2015225
Adverse EventStart DateEnd DateTime related to study treatmentCausality to study drugSeverity
OHSS09/08/201509/10/2015RelatedMild
Causality FactorsAction Taken with Study TreatmentOther action takenOutcomeAE Special InterestAE dose limiting toxicity
Protocol procedure**,Concomitant medication**(Othervalue:)Dose reducedLed to study terminationResolved
Event Description:abdominal distention;ascites;Drug:Hydroxyethyl Starch 130/0.4 and Sodium Chloride Injection 500ml,ivgtt bid calcium gluconate injection 10ml+dextrose injection 500ml ivgtt qd 19-Aug-2015 / 21-Aug-2015
Subject received concomitant medications:
Does the subject have any relevant past or present medical conditions:No
ConditionStart DateRelated to study conditionOngoing



08-JUN-16
Ying Zhong/EMR700623-541/C05-0117
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