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Index of reports
> Cases resulting in disability (2)
> Cases with Intra-Uterine Death (1)
Below is the selection of adverse event reports related to Actiq (Fentanyl Oral Transmucosal) that includes cases resulting in disability where reactions include intra-uterine death.
Adverse event in 43 year old female receiving Actiq (Fentanyl Oral Transmucosal)
Reported by a consumer/non-health professional from United States on 2007-03-12
Patient: 43 year old female, weighing 54.4 kg (119.7 pounds)
Adverse reactions / side effects: Gastrointestinal Motility Disorder, Intra-Uterine Death, Drug Exposure Before Pregnancy, Constipation, Twin Pregnancy, Abdominal Discomfort, Drug Exposure During Pregnancy, Swelling, Hypertension, Cardiac Failure Congestive, Infarction
Adverse event resulted in: death, life threatening event, hospitalization, disablity
Suspect drug(s):
Duragesic-50
Dosage: patch see instructions transdermal
Indication: Abdominal Pain Upper
Duragesic-50
Dosage: patch see instructions transdermal
Indication: Gastrointestinal Disorder
Actiq
Dosage: 600 - 800mcg all day
Indication: Abdominal Pain Upper
Actiq
Dosage: 600 - 800mcg all day
Indication: Gastrointestinal Disorder
Actiq
Dosage: 600 - 800mcg all day
Indication: OFF Label USE
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