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Index of reports
> Cases resulting in life threatening events (13)
Below is the selection of adverse event reports related to Mobic (Meloxicam) that includes cases resulting in life threatening events.
Adverse event in female receiving Mobic (Meloxicam)
Reported by a physician from Australia on 2007-10-08
Patient: female, weighing 45.0 kg (99.0 pounds)
Adverse reactions / side effects: Gastric Ulcer Haemorrhage
Adverse event resulted in: life threatening event, hospitalization
Suspect drug(s):
Mobic (Meloxicam)
Adverse event in female receiving Mobic (Meloxicam)
Reported by a physician from Australia on 2007-10-04
Patient: female, weighing 45.0 kg (99.0 pounds)
Adverse reactions / side effects: Haemoptysis, Gastric Ulcer Haemorrhage
Adverse event resulted in: life threatening event, hospitalization
Suspect drug(s):
Mobic (Meloxicam)
Adverse event in 57 year old male receiving Mobic (Meloxicam)
Reported by a consumer/non-health professional from United States on 2007-10-02
Patient: 57 year old male, weighing 108.0 kg (237.5 pounds)
Adverse reactions / side effects: Toxic Epidermal Necrolysis, Pharyngitis Streptococcal, Scar, Stevens-Johnson Syndrome
Adverse event resulted in: life threatening event, hospitalization, disablity
Suspect drug(s):
Mobic (Meloxicam)
Adverse event in male receiving Mobic (Meloxicam)
Reported by a physician from Australia on 2007-07-27
Patient: male, weighing 82.0 kg (180.4 pounds)
Adverse reactions / side effects: Gastrointestinal Haemorrhage
Adverse event resulted in: life threatening event, hospitalization
Suspect drug(s):
Mobic
Administration route: Oral
Indication: Osteoarthritis
Start date: 2004-10-01
End date: 2007-06-01
Cartia XT
Administration route: Oral
Indication: Prophylaxis
Other drugs received by patient: Augmentin Forte (Amoxycillin)
Adverse event in 72 year old male receiving Mobic (Meloxicam)
Reported by a individual with unspecified qualification from United States on 2007-07-27
Patient: 72 year old male
Adverse reactions / side effects: Dizziness Exertional, Coronary Artery Disease, Procedural Dizziness
Adverse event resulted in: life threatening event, hospitalization
Suspect drug(s):
Mobic
Administration route: Oral
Indication: Osteoarthritis
Start date: 2007-04-17
Mobic
Other drugs received by patient: Glucosamine and Chondroitin; Alka Seltzer; Tums; Claritin; Bisacodyl; Tylenol (Caplet); Imodium
Adverse event in 55 year old female receiving Mobic (Meloxicam)
Reported by a pharmacist from United States on 2007-06-01
Patient: 55 year old female, weighing 56.0 kg (123.2 pounds)
Adverse reactions / side effects: Weight Decreased, Hepatitis C Antibody Positive, Dizziness Exertional, Chills, Blood Thyroid Stimulating Hormone Increased, Hepatitis, Weight Increased, Herpes Simplex DNA Test Positive, Fatigue, Skin Lesion, Oedema Peripheral, Liver Function Test Abnormal, Cold Sweat, Blister, Blood Urine Present, Urinary Tract Infection, Rash, Tenosynovitis, Burning Sensation, Fungal Infection, Memory Impairment, Asthenia, Influenza Like Illness
Adverse event resulted in: life threatening event, hospitalization, disablity
Suspect drug(s):
Mobic (Meloxicam)
Other drugs received by patient: Klonopin; Adderall 10; Zelnorm; Synthroid; Seroquel
Adverse event in 69 year old female receiving Mobic (Meloxicam)
Reported by a consumer/non-health professional from Japan on 2007-05-30
Patient: 69 year old female
Adverse reactions / side effects: Interstitial Lung Disease
Adverse event resulted in: life threatening event
Suspect drug(s):
Taxol
Indication: Uterine Cancer
Start date: 2005-08-25
End date: 2005-08-25
Paraplatin
Indication: Uterine Cancer
Start date: 2005-08-25
End date: 2005-08-25
Mobic
Administration route: Oral
Adverse event in 69 year old female receiving Mobic (Meloxicam)
Reported by a health professional (non-physician/pharmacist) from Japan on 2007-05-22
Patient: 69 year old female
Adverse reactions / side effects: Interstitial Lung Disease
Adverse event resulted in: life threatening event
Suspect drug(s):
Taxol
Indication: Uterine Cancer
Start date: 2005-08-25
End date: 2005-08-25
Paraplatin
Indication: Uterine Cancer
Start date: 2005-08-25
End date: 2005-08-25
Mobic
Administration route: Oral
Adverse event in male receiving Mobic (Meloxicam)
Reported by a physician from Australia on 2007-05-04
Patient: male, weighing 84.0 kg (184.8 pounds)
Adverse reactions / side effects: Duodenal Ulcer Haemorrhage
Adverse event resulted in: life threatening event, hospitalization
Suspect drug(s):
Mobic (Meloxicam)
Adverse event in male receiving Mobic (Meloxicam)
Reported by a physician from Australia on 2007-03-07
Patient: male, weighing 87.0 kg (191.4 pounds)
Adverse reactions / side effects: Hepatitis Cholestatic, Hepatitis, Nephritis
Adverse event resulted in: life threatening event
Suspect drug(s):
Mobic
Administration route: Oral
Indication: Osteoarthritis
Start date: 2000-06-15
End date: 2006-08-15
Atacand
Administration route: Oral
Indication: Essential Hypertension
Start date: 2005-06-15
End date: 2006-08-15
Sildenafil Citrate
Administration route: Oral
Indication: Somatoform Disorder
Start date: 2003-06-15
End date: 2006-08-15
Atenolol
Administration route: Oral
Indication: Essential Hypertension
Start date: 2004-06-15
End date: 2006-08-15
Atorvastatin
Administration route: Oral
Indication: Metabolic Disorder
Start date: 2004-06-15
End date: 2006-08-15
Rabeprazole Sodium
Administration route: Oral
Indication: Oesophageal Disorder
Start date: 2005-07-15
End date: 2006-08-15
Adverse event in male receiving Mobic (Meloxicam)
Reported by a physician from Australia on 2007-03-02
Patient: male, weighing 87.0 kg (191.4 pounds)
Adverse reactions / side effects: Hepatitis Cholestatic, Hepatitis, Nephritis
Adverse event resulted in: life threatening event
Suspect drug(s):
Mobic
Administration route: Oral
Indication: Osteoarthritis
Start date: 2000-06-15
End date: 2006-08-15
Atacand
Administration route: Oral
Indication: Somatoform Disorder
Start date: 2005-06-15
End date: 2006-08-15
Sildenafil Citrate
Administration route: Oral
Indication: Essential Hypertension
Start date: 2003-06-15
End date: 2006-08-15
Atenolol
Administration route: Oral
Indication: Metabolic Disorder
Start date: 2004-06-15
End date: 2006-08-15
Atorvastatin
Administration route: Oral
Indication: Essential Hypertension
Start date: 2004-06-15
End date: 2006-08-15
Rabeprazole Sodium
Administration route: Oral
Indication: Oesophageal Disorder
Start date: 2005-07-15
End date: 2006-08-15
Adverse event in male receiving Mobic (Meloxicam)
Reported by a individual with unspecified qualification from United States on 2007-02-15
Patient: male, weighing 79.4 kg (174.6 pounds)
Adverse reactions / side effects: Malaise, Ulcer Haemorrhage, Loss of Consciousness
Adverse event resulted in: death, life threatening event, hospitalization, disablity
Suspect drug(s):
Mobic (Meloxicam)
Other drugs received by patient: Hytrin; Doxycycline; Acetaminophen; Multi-Vitamin
Adverse event in male receiving Mobic (Meloxicam)
Reported by a physician from Australia on 2007-01-12
Patient: male, weighing 90.0 kg (198.0 pounds)
Adverse reactions / side effects: Pain in Extremity, Chest Pain, Cardiac Arrest
Adverse event resulted in: life threatening event
Suspect drug(s):
Mobic (Meloxicam)
Other drugs received by patient: Metoprolol Succinate; Epilim; Lipitor; Plavix; Ramipril; Aspirin; Luvox
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