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Index of reports
> Cases resulting in hospitalization (191)
Below is the selection of adverse event reports related to Oxycontin (Oxycodone) that includes cases resulting in hospitalization.
Reports 1 - 25 of 191 Next >>
Adverse event in 86 year old male receiving Oxycontin (Oxycodone)
Reported by a individual with unspecified qualification on 2007-10-26
Patient: 86 year old male
Adverse reactions / side effects: Electrocardiogram QT Prolonged, Confusional State, Hallucination, Visual, Diabetes Mellitus, Hallucination, Auditory
Adverse event resulted in: hospitalization
Suspect drug(s):
Oxycontin
Administration route: Oral
Indication: Back Pain
Start date: 2007-06-25
Deltison
Indication: Back Pain
Start date: 2007-06-25
Sotalol Hydrochloride
Indication: Drug USE FOR Unknown Indication
Other drugs received by patient: Impugan; Monoket; Laktulose ^dak^
Adverse event in female receiving Oxycontin (Oxycodone)
Reported by a individual with unspecified qualification from Japan on 2007-10-25
Patient: female
Adverse reactions / side effects: Pain in Extremity, Blood Lactate Dehydrogenase Increased, Protein Total Decreased, Cardiac Failure Acute, Aspartate Aminotransferase Increased, Protein Total Increased, Neutropenia, Blood Creatinine Increased, Leukopenia
Adverse event resulted in: death, hospitalization
Suspect drug(s):
Navelbine
Dosage: 25 mg/m2 iv
Indication: Breast Cancer Recurrent
Start date: 2007-08-21
End date: 2007-08-21
Adriamycin PFS
Indication: Breast Cancer Recurrent
Hysron. Mfr: NOT Specified
Indication: Drug USE FOR Unknown Indication
Loxonin. Mfr: NOT Specified
Dosage: 180 mg qd po
Administration route: Oral
Indication: Drug USE FOR Unknown Indication
Oxycontin
Dosage: 80 mg qd po
Administration route: Oral
Indication: Drug USE FOR Unknown Indication
Other drugs received by patient: Taxol
Adverse event in 59 year old male receiving Oxycontin (Oxycodone)
Reported by a individual with unspecified qualification from United States on 2007-10-23
Patient: 59 year old male, weighing 95.0 kg (209.0 pounds)
Adverse reactions / side effects: Back Pain, Abdominal Distension
Adverse event resulted in: hospitalization
Suspect drug(s):
Oxycontin
Dosage: 20 mg, q8h
Administration route: Oral
Indication: Drug USE FOR Unknown Indication
Start date: 2007-01-04
End date: 2007-02-06
AG-013, 736
Dosage: 10 mg, daily
Indication: Renal Cell Carcinoma Stage Unspecified
Start date: 2006-11-20
Other drugs received by patient: Zocor; Tricor; Altace; Coreg; Norvasc; Hydralazine HCL; Doxazosin Mesylate; Colace Capsules
Adverse event in female receiving Oxycontin (Oxycodone)
Reported by a individual with unspecified qualification on 2007-10-19
Patient: female, weighing 82.0 kg (180.4 pounds)
Adverse reactions / side effects: Tooth Loss, Personality Change, Pain, Somnolence, Suicidal Ideation, Speech Disorder, Thinking Abnormal, Bipolar I Disorder, Impaired Self-Care, Anger, Unevaluable Event, Spousal Abuse, Dyspnoea, Nightmare, Motor Dysfunction, General Physical Health Deterioration, Abnormal Behaviour, Drug Withdrawal Syndrome, Amnesia, Discomfort, Aggression, Tremor, Mental Impairment, Insomnia, Mental Disorder, Homicidal Ideation, Drug Dependence, Delusional Perception
Adverse event resulted in: hospitalization, disablity
Suspect drug(s):
Oxycontin (Oxycodone)
Other drugs received by patient: Nexium; Soma; Lunesta; Maxzide; Zyrtec; Synthroid; Lyrica; Propranolol
Adverse event in male receiving Oxycontin (Oxycodone)
Reported by a individual with unspecified qualification on 2007-10-18
Patient: male
Adverse reactions / side effects: Renal Failure, Hepatic Failure, Neoplasm, Cardiac Disorder
Adverse event resulted in: hospitalization
Suspect drug(s):
Oxycontin (Oxycodone)
Adverse event in 49 year old male receiving Oxycontin (Oxycodone)
Reported by a individual with unspecified qualification on 2007-10-18
Patient: 49 year old male
Adverse reactions / side effects: Confusional State, Hypotension, Coma, Disorientation, Respiratory Depression, Extensor Plantar Response
Adverse event resulted in: hospitalization
Suspect drug(s):
Oxycontin
Dosage: 80 mg, daily
Administration route: Oral
Indication: Metastatic Pain
Start date: 2007-07-01
Oxycontin
Dosage: 80 mg, bid
Administration route: Oral
Start date: 2007-08-22
Oxynorm Capsules 20 MG
Dosage: 20 mg, prn
Administration route: Oral
Indication: Metastatic Pain
Start date: 2007-07-01
Tranxene
Dosage: 1 df, daily
Administration route: Oral
Indication: Metastatic Pain
End date: 2007-08-29
Other drugs received by patient: Taxol; Taxol; Solu-Medrol; Polaramine; Cimetidine; Zofran; Cortancyl; Paracetamol; Lyrica; Inipomp; Duphalac; Carboplatin; Carboplatin; Carboplatin; Tranxene
Adverse event in female receiving Oxycontin (Oxycodone)
Reported by a individual with unspecified qualification on 2007-10-18
Patient: female
Adverse reactions / side effects: Hospitalisation, Drug Dependence
Adverse event resulted in: hospitalization
Suspect drug(s):
Oxycontin (Oxycodone)
Adverse event in 72 year old male receiving Oxycontin (Oxycodone)
Reported by a individual with unspecified qualification on 2007-10-17
Patient: 72 year old male
Adverse reactions / side effects: Confusional State, Atrial Fibrillation, Somnolence, Fall, Loss of Consciousness, Fatigue, Dizziness, Gait Disturbance, Hallucination
Adverse event resulted in: death, hospitalization
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 83 year old female receiving Oxycontin (Oxycodone)
Reported by a individual with unspecified qualification on 2007-10-16
Patient: 83 year old female
Adverse reactions / side effects: Confusional State, Renal Failure Acute
Adverse event resulted in: hospitalization
Suspect drug(s):
Oxycontin
Dosage: 5 mg, daily
Administration route: Oral
Indication: Arthralgia
Start date: 2007-07-09
End date: 2007-07-26
Oxynorm Capsules 5 MG
Dosage: 5 mg, prn
Administration route: Oral
Indication: Arthralgia
Start date: 2007-07-09
End date: 2007-07-26
Other drugs received by patient: Plavix; Kardegic; Tenormin; Tahor; Isocard; Perindopril Erbumine; Temesta; Zoloft; Esomeprazole; Sodium Alginate; Duphalac; Primperan; Forlax; MAG 2; Diffu K; Zometa
Adverse event in 80 year old female receiving Oxycontin (Oxycodone)
Reported by a individual with unspecified qualification on 2007-10-15
Patient: 80 year old female
Adverse reactions / side effects: Large Intestine Perforation, Faecaloma
Adverse event resulted in: death, hospitalization
Suspect drug(s):
Oxycontin
Dosage: unk mg, unk
Administration route: Oral
Indication: Drug USE FOR Unknown Indication
Percocet
Dosage: unk mg, unk
Administration route: Oral
Indication: Drug USE FOR Unknown Indication
Adverse event in male receiving Oxycontin (Oxycodone)
Reported by a individual with unspecified qualification on 2007-10-15
Patient: male
Adverse reactions / side effects: Drug Effect Decreased, Skin Disorder, Drug Withdrawal Syndrome, Fall, Constipation, Cardiomegaly, Pericardial Effusion, Balance Disorder, Oedema Peripheral, Gastrointestinal Disorder, Gastrointestinal Obstruction, Neuromyopathy
Adverse event resulted in: hospitalization
Suspect drug(s):
Oxycontin (Oxycodone)
Other drugs received by patient: Relafen; Bupropion HCL; Lortab; Elmiron; Cozaar; Lexapro; Vioxx
Adverse event in male receiving Oxycontin (Oxycodone)
Reported by a individual with unspecified qualification on 2007-10-15
Patient: male
Adverse reactions / side effects: Hospitalisation, Pain, Drug Withdrawal Syndrome, Drug Dependence, Mobility Decreased
Adverse event resulted in: hospitalization
Suspect drug(s):
Oxycontin (Oxycodone)
Other drugs received by patient: Hydrocodone; Vitamins
Adverse event in male receiving Oxycontin (Oxycodone)
Reported by a individual with unspecified qualification on 2007-10-12
Patient: male
Adverse reactions / side effects: Anxiety Disorder, Cerebral Disorder, Malnutrition, Encephalopathy, Constipation, Suicidal Ideation, Impaired Driving Ability, Cluster Headache, Malaise, Road Traffic Accident, Euphoric Mood, Alcoholism, Major Depression, Hypertension, Drug Dependence, Crying
Adverse event resulted in: hospitalization, disablity
Suspect drug(s):
Oxycontin (Oxycodone)
Other drugs received by patient: Oxyfast Concentrate 20 MG / ML; Vioxx; Neurontin; Lexapro; Seroquel; Trazodone HCL; Synthroid; Trandate; Levoxyl; Atarax; Folic Acid
Adverse event in male receiving Oxycontin (Oxycodone)
Reported by a individual with unspecified qualification on 2007-10-10
Patient: male
Adverse reactions / side effects: Pruritus, Drug Withdrawal Syndrome, Self Injurious Behaviour, Somnolence, Suicidal Ideation, Social Problem, Road Traffic Accident, Overdose, Drug Dependence
Adverse event resulted in: hospitalization
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):
Zometa
Dosage: 4 mg, unk
Indication: Metastases TO Bone
Start date: 2006-11-14
End date: 2007-01-09
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
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
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
TS 1
Dosage: 100 mg/d
Administration route: Oral
Indication: Metastases TO Bone
Start date: 2006-04-05
End date: 2006-10-31
Krestin
Dosage: 3 g/d
Administration route: Oral
Indication: Metastases TO Bone
Start date: 2006-07-26
End date: 2006-10-31
DAI-Kenchu-TO
Dosage: 2.5 g/d
Administration route: Oral
Indication: Constipation
Start date: 2006-11-28
End date: 2006-12-20
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 2007-10-09
Patient: male, weighing 117.0 kg (257.4 pounds)
Adverse reactions / side effects: Tooth Loss, Bedridden, Pain, Drug Abuser, Libido Decreased, Drug Withdrawal Syndrome, Abdominal Wound Dehiscence, Surgery, Malaise, Myocardial Infarction, Drug Dependence
Adverse event resulted in: hospitalization
Suspect drug(s):
Oxycontin (Oxycodone)
Other drugs received by patient: Oxyir; Ativan; Bactrim; Neurontin
Adverse event in male receiving Oxycontin (Oxycodone)
Reported by a individual with unspecified qualification on 2007-10-04
Patient: male
Adverse reactions / side effects: Vomiting, Hospitalisation, Chest Pain, Drug Withdrawal Syndrome, Drug Dependence
Adverse event resulted in: hospitalization
Suspect drug(s):
Oxycontin (Oxycodone)
Adverse event in female receiving Oxycontin (Oxycodone)
Reported by a individual with unspecified qualification on 2007-10-04
Patient: female
Adverse reactions / side effects: Large Intestine Perforation, Faecaloma
Adverse event resulted in: death, hospitalization
Suspect drug(s):
Oxycontin (Oxycodone)
Adverse event in 40 year old male receiving Oxycontin (Oxycodone)
Reported by a individual with unspecified qualification on 2007-10-04
Patient: 40 year old male
Adverse reactions / side effects: Coma
Adverse event resulted in: hospitalization
Suspect drug(s):
Oxycontin
Dosage: 10 mg, bid
Administration route: Oral
Indication: Pain
Start date: 2007-09-01
End date: 2007-09-17
Oxycontin
Dosage: 20 mg, pm
Administration route: Oral
Start date: 2007-09-17
End date: 2007-09-17
Other drugs received by patient: Oxynorm Capsules 5 MG
Adverse event in male receiving Oxycontin (Oxycodone)
Reported by a individual with unspecified qualification on 2007-10-03
Patient: male
Adverse reactions / side effects: Unresponsive TO Stimuli, Loss of Consciousness
Adverse event resulted in: hospitalization
Suspect drug(s):
Oxycontin (Oxycodone)
Other drugs received by patient: Zoloft; Nexium; Aldactone; Ambien; Flexeril; Docusate; Furosemide; Lactulose
Adverse event in female receiving Oxycontin (Oxycodone)
Reported by a health professional (non-physician/pharmacist) from France on 2007-10-03
Patient: female
Adverse reactions / side effects: Drug Dependence
Adverse event resulted in: hospitalization
Suspect drug(s):
Effexor XR
Dosage: unknown
Administration route: Oral
Indication: Depression
Rivotril
Dosage: unknown
Administration route: Oral
Indication: Neuralgia
Atarax
Dosage: unknown
Administration route: Oral
Indication: Anxiety
Lexomil
Dosage: unknown
Administration route: Oral
Indication: Anxiety
Oxycontin
Dosage: unknown
Administration route: Oral
Indication: Pain
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):
Zometa
Dosage: 4 mg, unk
Indication: Metastases TO Bone
Start date: 2006-11-14
End date: 2007-01-09
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
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
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
TS 1
Dosage: 100 mg/d
Administration route: Oral
Indication: Metastases TO Bone
Start date: 2006-04-05
End date: 2006-10-31
Krestin
Dosage: 3 g/d
Administration route: Oral
Indication: Metastases TO Bone
Start date: 2006-07-26
End date: 2006-10-31
DAI-Kenchu-TO
Dosage: 2.5 g/d
Administration route: Oral
Indication: Constipation
Start date: 2006-11-28
End date: 2006-12-20
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 2007-10-02
Patient: male
Adverse reactions / side effects: General Physical Health Deterioration, Drug Withdrawal Syndrome, Amnesia, Weight Increased, Anxiety, Drug Tolerance, Disturbance in Attention, Unevaluable Event, Depression, Drug Dependence
Adverse event resulted in: hospitalization
Suspect drug(s):
Oxycontin (Oxycodone)
Adverse event in 68 year old male receiving Oxycontin (Oxycodone)
Reported by a individual with unspecified qualification on 2007-10-01
Patient: 68 year old male, weighing 68.0 kg (149.6 pounds)
Adverse reactions / side effects: Dyspnoea, Pneumonia, Hypotension, Mental Status Changes, Drug Interaction, Somnolence, Speech Disorder, Anxiety, Psychotic Disorder, Dyspepsia, Heart Rate Irregular, Bradycardia, Hallucination
Adverse event resulted in: hospitalization
Suspect drug(s):
Oxycontin
Dosage: unk, unk
Administration route: Oral
Indication: Drug USE FOR Unknown Indication
Start date: 2006-02-21
AG-013, 736
Dosage: 10 mg, daily
Administration route: Oral
Indication: Pancreatic Carcinoma
Start date: 2006-02-27
End date: 2006-04-05
Lorazepam
Dosage: unk, unk
Administration route: Oral
Indication: Anxiety
Start date: 2006-03-24
Other drugs received by patient: Lactulose; Carvedilol; Divalproex Sodium; Aspirin; Vitamin CAP; Vitamin B; Tamsulosin HCL; Simvastatin; Nexium; Oxycodone HCL; Levaquin; Zoloft
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