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Cervidil (Dinoprostone Vaginal) - Adverse Event Reports - Serious Event

 



Index of reports > Cases resulting in a serious event (8)

     Drug Exposure During Pregnancy (6)Caesarean Section (4)Apgar Score LOW (2)Uterine Atony (2)Nuclear Magnetic Resonance Imaging Brain Abnormal (2)Meningism (2)Convulsion (2)Tachycardia Foetal (2)Reversible Posterior Leukoencephalopathy Syndrome (2)Premature Separation of Placenta (2)

Below is the selection of adverse event reports related to Cervidil (Dinoprostone Vaginal) that includes cases resulting in a serious event.

Adverse event in 26 year old female receiving Cervidil (Dinoprostone Vaginal)

Reported by a consumer/non-health professional from United States on 2007-07-20

Patient: 26 year old female

Adverse reactions / side effects: Rubella Antibody Positive, Inappropriate Schedule of Drug Administration, Drug Dose Omission, Drug Exposure During Pregnancy, Heart Rate Increased, Amniocentesis Abnormal, Pregnancy

Suspect drug(s):
Cervidil

Claravis
    Dosage: 40 mg, bid, oral
    Administration route: Oral
    Start date: 2006-02-07
    End date: 2006-08-13

Ortho TRI-Cyclen LO
    Dosage: 1 tablet, qd, oral
    Administration route: Oral
    Indication: Oral Contraception

Other drugs received by patient: Chitosan (Poliglusam); Isotrim (Sulfamethoxazole, Trimethoprim); Vita-PAK



Adverse event in 30 year old female receiving Cervidil (Dinoprostone Vaginal)

Reported by a individual with unspecified qualification from United Kingdom on 2007-07-06

Patient: 30 year old female, weighing 71.5 kg (157.3 pounds)

Adverse reactions / side effects: Postpartum Haemorrhage, Caesarean Section, Apgar Score LOW, Body Temperature Increased, Drug Exposure During Pregnancy, Foetal Heart Rate Deceleration, Uterine Atony, Foetal Heart Rate Abnormal, Tachycardia Foetal

Adverse event resulted in: life threatening event, hospitalization, disablity

Suspect drug(s):
Cervidil (Dinoprostone Vaginal)

Other drugs received by patient: Zolpidem Tartrate; Tylenol (Caplet); Intravenous Fluids; Epidural OR Regional Anesthesia; Oxygen



Adverse event in male receiving Cervidil (Dinoprostone Vaginal)

Reported by a individual with unspecified qualification from United Kingdom on 2007-07-06

Patient: male, weighing 2.5 kg (5.4 pounds)

Adverse reactions / side effects: Apgar Score LOW, Caesarean Section, Drug Exposure During Pregnancy, Foetal Heart Rate Disorder, PRE-Eclampsia, Tachycardia Foetal

Adverse event resulted in: hospitalization

Suspect drug(s):
Cervidil
    Dosage: 10 mg once transplacental
    Indication: Labour Induction
    Start date: 2006-12-27
    End date: 2006-12-27

Cervidil
    Dosage: 10 mg once transplacental
    Indication: Uterine Cervix Dilation Procedure
    Start date: 2006-12-27
    End date: 2006-12-27

Other drugs received by patient: Zolpidem Tartrate; Tylenol (Caplet); Intravenous Fluids; Epidural OR Regional Anesthesia; Oxygen



Adverse event in 30 year old female receiving Cervidil (Dinoprostone Vaginal)

Reported by a individual with unspecified qualification from United Kingdom on 2007-06-27

Patient: 30 year old female, weighing 71.5 kg (157.3 pounds)

Adverse reactions / side effects: Placental Infarction, Uterine Atony, Haemoglobin Decreased, Caesarean Section, Haematocrit Decreased, Drug Exposure During Pregnancy, NO Therapeutic Response, Surgical Failure, PRE-Eclampsia

Adverse event resulted in: life threatening event, hospitalization, disablity

Suspect drug(s):
Cervidil (Dinoprostone Vaginal)

Other drugs received by patient: Zolpidem Tartrate; Tylenol (Caplet)



Adverse event in female receiving Cervidil (Dinoprostone Vaginal)

Reported by a health professional (non-physician/pharmacist) from France on 2007-06-04

Patient: female

Adverse reactions / side effects: Vomiting, Nuclear Magnetic Resonance Imaging Brain Abnormal, Meningism, Postictal State, Convulsion, Reversible Posterior Leukoencephalopathy Syndrome, Drug Exposure During Pregnancy, Tetanus, Tongue Biting, Musculoskeletal Stiffness

Adverse event resulted in: hospitalization

Suspect drug(s):
Cervidil
    Dosage: 10 mg once vg
    Indication: Uterine Cervix Dilation Procedure
    Start date: 2007-02-09

Syntocinon
    Indication: Labour Induction
    Start date: 2007-02-09

Other drugs received by patient: Salbutamol



Adverse event in female receiving Cervidil (Dinoprostone Vaginal)

Reported by a individual with unspecified qualification from United Kingdom on 2007-05-23

Patient: female

Adverse reactions / side effects: Reversible Posterior Leukoencephalopathy Syndrome, Nuclear Magnetic Resonance Imaging Brain Abnormal, Meningism, Convulsion

Adverse event resulted in: hospitalization

Suspect drug(s):
Cervidil
    Dosage: 10 mg once vg
    Indication: Cervix Disorder
    Start date: 2007-02-09

Syntocinon
    Indication: Labour Induction
    Start date: 2007-02-09

Other drugs received by patient: Salbutamol



Adverse event in female receiving Cervidil (Dinoprostone Vaginal)

Reported by a health professional (non-physician/pharmacist) from Canada on 2007-03-09

Patient: female

Adverse reactions / side effects: Caesarean Section, Drug Exposure During Pregnancy, Premature Separation of Placenta

Adverse event resulted in: hospitalization

Suspect drug(s):
Cervidil (Dinoprostone Vaginal)



Adverse event in female receiving Cervidil (Dinoprostone Vaginal)

Reported by a health professional (non-physician/pharmacist) from Canada on 2007-03-09

Patient: female

Adverse reactions / side effects: Premature Separation of Placenta

Suspect drug(s):
Cervidil (Dinoprostone Vaginal)

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