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Actiq (Fentanyl Oral Transmucosal) - Adverse Event Reports - Life Threatening Events

 



Index of reports > Cases resulting in life threatening events (6)

     Coma (4)Incorrect Dose Administered (2)Acidosis (2)Respiratory Depression (2)Convulsion (2)Irritability (2)Cyanosis (2)Respiratory Arrest (2)Hypertension (2)Accidental Drug Intake by Child (2)

Below is the selection of adverse event reports related to Actiq (Fentanyl Oral Transmucosal) that includes cases resulting in life threatening events.

Adverse event in 70 year old male receiving Actiq (Fentanyl Oral Transmucosal)

Reported by a health professional (non-physician/pharmacist) from United Kingdom on 2007-10-08

Patient: 70 year old male

Adverse reactions / side effects: Overdose, Medication Error, Intentional Drug Misuse

Adverse event resulted in: life threatening event, hospitalization

Suspect drug(s):
Actiq
    Indication: Pain

Fentanyl
    Indication: Pain



Adverse event in 1 year old female receiving Actiq (Fentanyl Oral Transmucosal)

Reported by a health professional (non-physician/pharmacist) from United States on 2007-07-10

Patient: 1 year old female

Adverse reactions / side effects: Cyanosis, Respiratory Arrest, Coma, Accidental Drug Intake by Child

Adverse event resulted in: life threatening event, hospitalization

Suspect drug(s):
Actiq (Fentanyl Oral Transmucosal)



Adverse event in 19 year old male receiving Actiq (Fentanyl Oral Transmucosal)

Reported by a health professional (non-physician/pharmacist) from United States on 2007-07-10

Patient: 19 year old male

Adverse reactions / side effects: Agitation, Blood Creatine Phosphokinase Increased, Incorrect Dose Administered, Alanine Aminotransferase Increased, Hypotension, Coma, Respiratory Depression, Acidosis, Convulsion, Irritability, Cyanosis, Aspartate Aminotransferase Increased

Adverse event resulted in: life threatening event, hospitalization

Suspect drug(s):
Actiq (Fentanyl Oral Transmucosal)



Adverse event in 16 month old female receiving Actiq (Fentanyl Oral Transmucosal)

Reported by a health professional (non-physician/pharmacist) from United States on 2007-07-10

Patient: 16 month old female

Adverse reactions / side effects: Mydriasis, Tachycardia, Coma, Acidosis, Muscle Rigidity, Convulsion, Coordination Abnormal, Hypertension, Accidental Drug Intake by Child, Pneumonitis

Adverse event resulted in: life threatening event, hospitalization

Suspect drug(s):
Actiq (Fentanyl Oral Transmucosal)



Adverse event in 59 year old female receiving Actiq (Fentanyl Oral Transmucosal)

Reported by a health professional (non-physician/pharmacist) from United States on 2007-07-10

Patient: 59 year old female

Adverse reactions / side effects: Agitation, Incorrect Dose Administered, Pain, Coma, Respiratory Depression, Somnolence, Irritability, Syncope, Suicide Attempt, Respiratory Arrest, Lethargy

Adverse event resulted in: life threatening event, hospitalization

Suspect drug(s):
Actiq (Fentanyl Oral Transmucosal)



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):
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

Duragesic-50
    Dosage: patch see instructions transdermal
    Indication: Abdominal Pain Upper

Duragesic-50
    Dosage: patch see instructions transdermal
    Indication: Gastrointestinal Disorder

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