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Index of reports
> Cases resulting in life threatening events (43)
Below is the selection of adverse event reports related to Oxycontin (Oxycodone) that includes cases resulting in life threatening events.
Reports 1 - 25 of 43 Next >>
Adverse event in 76 year old female receiving Oxycontin (Oxycodone)
Reported by a individual with unspecified qualification on 2007-10-31
Patient: 76 year old female
Adverse reactions / side effects: Bradypnoea, Miosis, Unresponsive TO Stimuli, Coma, Corneal Reflex Decreased
Adverse event resulted in: life threatening event
Suspect drug(s):
Morphine
Dosage: 1/2 vial
Indication: Pain
Oxycontin
Dosage: 20 mg, bid
Administration route: Oral
Indication: Pain
Adverse event in male receiving Oxycontin (Oxycodone)
Reported by a individual with unspecified qualification on 2007-10-19
Patient: male
Adverse reactions / side effects: Stupor, Suicidal Ideation, Aggression, Overdose, Road Traffic Accident, Respiratory Arrest, Mental Disorder, Drug Dependence
Adverse event resulted in: life threatening event
Suspect drug(s):
Oxycontin (Oxycodone)
Adverse event in 40 year old female receiving Oxycontin (Oxycodone)
Reported by a individual with unspecified qualification on 2007-10-18
Patient: 40 year old female
Adverse reactions / side effects: Cardiac Arrest
Adverse event resulted in: life threatening event
Suspect drug(s):
Oxycontin (Oxycodone)
Adverse event in 52 year old male receiving Oxycontin (Oxycodone)
Reported by a individual with unspecified qualification on 2007-10-17
Patient: 52 year old male
Adverse reactions / side effects: Nerve Injury, Rhabdomyolysis, Dementia, Impaired Work Ability, Fall, Amnesia, Loss of Consciousness, Overdose, Senile Psychosis, Muscle Injury, Rotator Cuff Syndrome
Adverse event resulted in: life threatening event, hospitalization, disablity
Suspect drug(s):
Oxycontin (Oxycodone)
Other drugs received by patient: Klonopin; Vistaril; Baclofen
Adverse event in 18 month old male receiving Oxycontin (Oxycodone)
Reported by a individual with unspecified qualification on 2007-10-16
Patient: 18 month old male
Adverse reactions / side effects: Overdose, Respiratory Arrest, Loss of Consciousness
Adverse event resulted in: life threatening event
Suspect drug(s):
Oxycontin (Oxycodone)
Adverse event in 61 year old male receiving Oxycontin (Oxycodone)
Reported by a individual with unspecified qualification from Japan on 2007-10-09
Patient: 61 year old male, weighing 48.0 kg (105.6 pounds)
Adverse reactions / side effects: Pyrexia, Hepatitis, Liver Disorder, Chest X-RAY Abnormal, Interstitial Lung Disease, Gamma-Glutamyltransferase Increased, Malignant Pleural Effusion, Blood Alkaline Phosphatase Increased, Dyspnoea, Blood Lactate Dehydrogenase Increased, Alanine Aminotransferase Increased, Localised Oedema, Pancytopenia, Lymphangiosis Carcinomatosa, Respiratory Distress, Computerised Tomogram Abnormal, Aspartate Aminotransferase Increased, Anorexia
Adverse event resulted in: death, life threatening event, hospitalization
Suspect drug(s):
Cddp + Etoposide+ctx+mtx+5-Fu+adr+vcr
Dosage: 50 mg/d
Indication: Metastases TO Bone
Start date: 2006-11-24
End date: 2006-12-08
CPT-11
Dosage: 100 mg/d
Indication: Metastases TO Bone
Start date: 2006-11-24
End date: 2006-11-24
CPT-11
Dosage: 50 mg/d
Start date: 2006-12-08
End date: 2006-12-08
DAI-Kenchu-TO
Dosage: 2.5 g/d
Administration route: Oral
Indication: Constipation
Start date: 2006-11-28
End date: 2006-12-20
Krestin
Dosage: 3 g/d
Administration route: Oral
Indication: Metastases TO Bone
Start date: 2006-07-26
End date: 2006-10-31
Oxycontin
Dosage: 45 mg/d
Administration route: Oral
Indication: Cancer Pain
Start date: 2006-11-15
Relifen
Dosage: 800 mg/d
Administration route: Oral
Indication: Cancer Pain
Start date: 2006-11-14
End date: 2007-02-01
TS 1
Dosage: 100 mg/d
Administration route: Oral
Indication: Metastases TO Bone
Start date: 2006-04-05
End date: 2006-10-31
Zometa
Dosage: 4 mg, unk
Indication: Metastases TO Bone
Start date: 2006-11-14
End date: 2007-01-09
Other drugs received by patient: Camptosar; Cisplatin; Mucosta; Novamin; Primperan; Maglax
Adverse event in 46 year old male receiving Oxycontin (Oxycodone)
Reported by a individual with unspecified qualification on 2007-10-08
Patient: 46 year old male
Adverse reactions / side effects: Homicide, Thinking Abnormal, Injury
Adverse event resulted in: life threatening event, disablity
Suspect drug(s):
Oxycontin (Oxycodone)
Adverse event in 18 month old male receiving Oxycontin (Oxycodone)
Reported by a individual with unspecified qualification on 2007-10-04
Patient: 18 month old male
Adverse reactions / side effects: Loss of Consciousness
Adverse event resulted in: life threatening event
Suspect drug(s):
Oxycontin (Oxycodone)
Adverse event in 61 year old male receiving Oxycontin (Oxycodone)
Reported by a individual with unspecified qualification on 2007-10-02
Patient: 61 year old male
Adverse reactions / side effects: Cholestasis
Adverse event resulted in: life threatening event
Suspect drug(s):
Imunace
Dosage: 700 kiu, daily
Indication: Renal Cell Carcinoma Stage IV
Start date: 2007-07-26
End date: 2007-08-09
Oxycontin
Dosage: 5 mg, bid
Indication: Cancer Pain
Start date: 2007-08-02
End date: 2007-08-14
Other drugs received by patient: Tagamet; Loxonin; Mucosta; Pantosin; Codeine Phosphate; Magnesium Oxide; Napa; Napa; Ceftazidime; Novamin; Fentanyl
Adverse event in 61 year old male receiving Oxycontin (Oxycodone)
Reported by a individual with unspecified qualification from Japan on 2007-10-02
Patient: 61 year old male, weighing 48.0 kg (105.6 pounds)
Adverse reactions / side effects: Pyrexia, Hepatitis, Liver Disorder, Gamma-Glutamyltransferase Increased, Interstitial Lung Disease, Malignant Pleural Effusion, Blood Alkaline Phosphatase Increased, Dyspnoea, Blood Lactate Dehydrogenase Increased, Alanine Aminotransferase Increased, Pancytopenia, Localised Oedema, Lymphangiosis Carcinomatosa, Computerised Tomogram Abnormal, Anorexia, Aspartate Aminotransferase Increased
Adverse event resulted in: death, life threatening event, hospitalization
Suspect drug(s):
Cddp + Etoposide+ctx+mtx+5-Fu+adr+vcr
Dosage: 50 mg/d
Indication: Metastases TO Bone
Start date: 2006-11-24
End date: 2006-12-08
CPT-11
Dosage: 100 mg/d
Indication: Metastases TO Bone
Start date: 2006-11-24
End date: 2006-11-24
CPT-11
Dosage: 50 mg/d
Start date: 2006-12-08
End date: 2006-12-08
DAI-Kenchu-TO
Dosage: 2.5 g/d
Administration route: Oral
Indication: Constipation
Start date: 2006-11-28
End date: 2006-12-20
Krestin
Dosage: 3 g/d
Administration route: Oral
Indication: Metastases TO Bone
Start date: 2006-07-26
End date: 2006-10-31
Oxycontin
Dosage: 45 mg/d
Administration route: Oral
Indication: Cancer Pain
Start date: 2006-11-15
Relifen
Dosage: 800 mg/d
Administration route: Oral
Indication: Cancer Pain
Start date: 2006-11-14
End date: 2007-02-01
TS 1
Dosage: 100 mg/d
Administration route: Oral
Indication: Metastases TO Bone
Start date: 2006-04-05
End date: 2006-10-31
Zometa
Dosage: 4 mg, unk
Indication: Metastases TO Bone
Start date: 2006-11-14
End date: 2007-01-09
Other drugs received by patient: Camptosar; Cisplatin; Mucosta; Novamin; Primperan; Maglax
Adverse event in male receiving Oxycontin (Oxycodone)
Reported by a individual with unspecified qualification on 2007-07-30
Patient: male
Adverse reactions / side effects: Nausea, Pain, Drug Withdrawal Syndrome, Headache, Anxiety, Insomnia, Depression, Drug Dependence
Adverse event resulted in: life threatening event, hospitalization
Suspect drug(s):
Oxycontin (Oxycodone)
Other drugs received by patient: Unknown
Adverse event in female receiving Oxycontin (Oxycodone)
Reported by a individual with unspecified qualification on 2007-07-27
Patient: female
Adverse reactions / side effects: General Physical Health Deterioration, Headache, Drug Dependence, Apnoea, Amnesia, Convulsion
Adverse event resulted in: life threatening event
Suspect drug(s):
Oxycontin (Oxycodone)
Adverse event in male receiving Oxycontin (Oxycodone)
Reported by a individual with unspecified qualification on 2007-07-26
Patient: male
Adverse reactions / side effects: Resuscitation
Adverse event resulted in: life threatening event
Suspect drug(s):
Oxycontin (Oxycodone)
Adverse event in male receiving Oxycontin (Oxycodone)
Reported by a individual with unspecified qualification from United States on 2007-07-25
Patient: male
Adverse reactions / side effects: Road Traffic Accident, Substance Abuse, Loss of Consciousness
Adverse event resulted in: life threatening event
Suspect drug(s):
Alcohol(ethanol)
Indication: Drug Abuser
Oxycontin
Indication: Drug Abuser
Xanax
Indication: Drug Abuser
Adverse event in male receiving Oxycontin (Oxycodone)
Reported by a individual with unspecified qualification on 2007-07-24
Patient: male
Adverse reactions / side effects: Suicide Attempt
Adverse event resulted in: life threatening event
Suspect drug(s):
Oxycontin (Oxycodone)
Adverse event in male receiving Oxycontin (Oxycodone)
Reported by a individual with unspecified qualification on 2007-07-24
Patient: male
Adverse reactions / side effects: Bloody Discharge, Pneumonia, Malaise, Hyperthermia, Drug Dependence
Adverse event resulted in: life threatening event
Suspect drug(s):
Oxycontin (Oxycodone)
Adverse event in male receiving Oxycontin (Oxycodone)
Reported by a individual with unspecified qualification on 2007-06-29
Patient: male
Adverse reactions / side effects: Hospitalisation, Nightmare, Unevaluable Event, Drug Dependence
Adverse event resulted in: life threatening event, hospitalization
Suspect drug(s):
Oxycontin (Oxycodone)
Adverse event in 32 year old male receiving Oxycontin (Oxycodone)
Reported by a consumer/non-health professional from United States on 2007-06-26
Patient: 32 year old male, weighing 158.8 kg (349.3 pounds)
Adverse reactions / side effects: Legal Problem, Drug Dependence
Adverse event resulted in: life threatening event, hospitalization
Suspect drug(s):
Oxycontin
Dosage: 1 tab twice per day po
Administration route: Oral
Indication: Back Disorder
Percocet-5
Dosage: 1-2 tabs every 4 hours po
Administration route: Oral
Indication: Back Disorder
Adverse event in female receiving Oxycontin (Oxycodone)
Reported by a consumer/non-health professional from United States on 2007-06-26
Patient: female, weighing 81.2 kg (178.6 pounds)
Adverse reactions / side effects: Narcolepsy, Impaired Work Ability, Pain, Breakthrough Pain, Drug Interaction, Amnesia, Tremor, Impaired Driving Ability, Dysarthria, Thinking Abnormal, Disturbance in Attention, Panic Reaction
Adverse event resulted in: life threatening event, hospitalization
Suspect drug(s):
Oxycontin
Dosage: 60 mgs bid po
Administration route: Oral
Indication: Pain
Start date: 2005-01-01
End date: 2007-04-26
Xanax
Dosage: .75 mgs 4 x per day po
Administration route: Oral
Indication: Anxiety
Start date: 2007-03-01
End date: 2007-04-26
Adverse event in male receiving Oxycontin (Oxycodone)
Reported by a individual with unspecified qualification on 2007-06-25
Patient: male
Adverse reactions / side effects: Pain, Respiratory Arrest, Cardiac Arrest, Tendonitis, Upper Extremity Mass
Adverse event resulted in: life threatening event
Suspect drug(s):
Anti-Inflammatory
Dosage: unk, unk
Indication: Tendonitis
Oxycontin
Dosage: unk mg, unk
Administration route: Oral
Indication: Pain
Percocet
Dosage: unk, unk
Indication: Pain
Prednisone TAB
Dosage: unk, unk
Indication: Drug USE FOR Unknown Indication
Adverse event in female receiving Oxycontin (Oxycodone)
Reported by a individual with unspecified qualification on 2007-06-22
Patient: female, weighing 170.0 kg (374.0 pounds)
Adverse reactions / side effects: Overdose, Unresponsive TO Stimuli, Hepatic Failure, Victim of Homicide, Cardiac Arrest, Substance Abuse
Adverse event resulted in: death, life threatening event, hospitalization
Suspect drug(s):
Oxycontin
Dosage: unk, unk
Indication: Pain
Tylenol
Dosage: unk, unk
Indication: Pain
Other drugs received by patient: Insulin; Asthma Medications
Adverse event in 74 year old male receiving Oxycontin (Oxycodone)
Reported by a individual with unspecified qualification from United States on 2007-06-22
Patient: 74 year old male, weighing 72.6 kg (159.7 pounds)
Adverse reactions / side effects: Blood Alkaline Phosphatase Increased, Blood Bilirubin Increased, Blood Urea Increased, Hepatic Failure, Ascites, Hepatic Enzyme Increased, Hepatic Encephalopathy, Fatigue, Dehydration, Blood Creatinine Increased, Asthenia
Adverse event resulted in: life threatening event, hospitalization
Suspect drug(s):
Oxycodone 5 MG
Dosage: 1 once or twice a day prn po
Administration route: Oral
Indication: Abdominal Pain Lower
Start date: 2006-11-20
End date: 2007-05-22
Oxycontin
Dosage: 1 every 12 hours every 12 hours po
Administration route: Oral
Indication: Metastatic Carcinoma of THE Bladder
Start date: 2007-05-05
End date: 2007-05-22
Other drugs received by patient: Carboplatin and Gemcitabine; Ondansetron; Megace; Marinol
Adverse event in male receiving Oxycontin (Oxycodone)
Reported by a consumer/non-health professional from United States on 2007-06-11
Patient: male
Adverse reactions / side effects: Overdose, Drug Dependence
Adverse event resulted in: life threatening event, hospitalization, disablity
Suspect drug(s):
Oxycontin (Oxycodone)
Adverse event in 19 year old male receiving Oxycontin (Oxycodone)
Reported by a individual with unspecified qualification on 2007-06-11
Patient: 19 year old male, weighing 100.0 kg (220.0 pounds)
Adverse reactions / side effects: Multiple Drug Overdose Accidental, Substance Abuse, Organ Failure
Adverse event resulted in: death, life threatening event
Suspect drug(s):
Amphetamine Sulfate
Indication: Drug Abuser
Antihistamines FOR Systemic USE
Indication: Drug Abuser
Cocaine
Indication: Drug Abuser
Heroin
Indication: Drug Abuser
Marijuana
Indication: Drug Abuser
Oxycontin
Indication: Drug Abuser
Phenylpropanolamine
Indication: Drug Abuser
Vicodin
Indication: Drug Abuser
Xanax
Indication: Drug Abuser
Adverse event in 19 year old male receiving Oxycontin (Oxycodone)
Reported by a consumer/non-health professional from United States on 2007-06-11
Patient: 19 year old male
Adverse reactions / side effects: Choking, Feeling Hot, Unresponsive TO Stimuli, Multiple Drug Overdose, Foaming AT Mouth, Substance Abuse
Adverse event resulted in: death, life threatening event
Suspect drug(s):
Alcohol (Ethanol)
Dosage: oral
Administration route: Oral
Indication: Alcohol USE
Start date: 2005-09-23
Oxycontin
Dosage: 80 mg, see text
Indication: Drug Abuser
Start date: 2005-09-23
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