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Index of reports
> Cases resulting in life threatening events (45)
Below is the selection of adverse event reports related to Avelox (Moxifloxacin) that includes cases resulting in life threatening events.
Reports 1 - 25 of 45 Next >>
Adverse event in 54 year old male receiving Avelox (Moxifloxacin)
Reported by a physician from Belgium on 2007-10-29
Patient: 54 year old male, weighing 80.0 kg (176.0 pounds)
Adverse reactions / side effects: Respiratory Arrest
Adverse event resulted in: death, life threatening event
Suspect drug(s):
Avelox
Dosage: total daily dose: 400 mg unit dose: 400 mg
Administration route: Oral
Indication: Chronic Obstructive Pulmonary Disease
Start date: 2007-08-01
End date: 2007-08-01
Avelox
Dosage: total daily dose: 400 mg unit dose: 400 mg
Administration route: Oral
Start date: 2007-04-04
End date: 2007-04-04
Adverse event in 64 year old male receiving Avelox (Moxifloxacin)
Reported by a health professional (non-physician/pharmacist) from Germany on 2007-10-22
Patient: 64 year old male, weighing 70.0 kg (154.0 pounds)
Adverse reactions / side effects: Henoch-Schonlein Purpura, Diarrhoea Haemorrhagic, Glomerulonephritis Rapidly Progressive, Rectal Tenesmus, Renal Failure Acute
Adverse event resulted in: life threatening event, hospitalization, disablity
Suspect drug(s):
Avelox (Moxifloxacin)
Other drugs received by patient: Concor COR; Aspirin
Adverse event in 82 year old female receiving Avelox (Moxifloxacin)
Reported by a physician from Netherlands on 2007-10-18
Patient: 82 year old female, weighing 62.0 kg (136.4 pounds)
Adverse reactions / side effects: Anaphylactic Reaction, Circulatory Collapse, Cardiac Arrest, Laryngeal Disorder
Adverse event resulted in: death, life threatening event, hospitalization
Suspect drug(s):
Avelox (Moxifloxacin)
Other drugs received by patient: Zocor; Zocor; Selokeen ZOC; Selokeen ZOC; Captopril; Monocedocard Retard; Acetosal; Losec; Cordarone; Serevent; Atrovent; Spiriva; Lasix; Mogadon; Doxycycline; Prednison; Prednison; Prednison; Noroxin
Adverse event in 37 year old male receiving Avelox (Moxifloxacin)
Reported by a physician from Germany on 2007-10-18
Patient: 37 year old male, weighing 63.0 kg (138.6 pounds)
Adverse reactions / side effects: Thrombotic Thrombocytopenic Purpura
Adverse event resulted in: life threatening event
Suspect drug(s):
Avelox
Administration route: Oral
Start date: 2007-03-03
End date: 2007-03-07
Moxifloxacin HCL
Administration route: Oral
Indication: Bronchitis
Start date: 2007-01-22
End date: 2007-01-31
Piperacillin
Start date: 2007-03-02
End date: 2007-03-09
Other drugs received by patient: Pantoprazole Sodium; Pantoprazole Sodium; Calcilac; Combactam; Decortin H; Paracetamol; Paracetamol; Faktu; Doloproct; Hametum; Aspirin; Ibuprofen
Adverse event in 93 year old female receiving Avelox (Moxifloxacin)
Reported by a physician from Italy on 2007-10-01
Patient: 93 year old female
Adverse reactions / side effects: Jaundice, Hepatitis Acute, Xerophthalmia, Cytolytic Hepatitis, Cholestasis
Adverse event resulted in: life threatening event
Suspect drug(s):
Avelox
Dosage: total daily dose: 400 mg unit dose: 400 mg
Administration route: Oral
Indication: Bronchopneumonia
Start date: 2007-08-28
End date: 2007-09-06
Fidato
Dosage: total daily dose: 2 g unit dose: 2 g
Indication: Bronchopneumonia
Start date: 2007-08-18
End date: 2007-09-07
Tavanic
Dosage: total daily dose: 500 mg unit dose: 500 mg
Indication: Bronchopneumonia
Start date: 2007-08-22
End date: 2007-08-27
Other drugs received by patient: Enoxaparin Sodium; Lanoxin
Adverse event in 77 year old male receiving Avelox (Moxifloxacin)
Reported by a physician from Japan on 2007-07-25
Patient: 77 year old male
Adverse reactions / side effects: Hypoglycaemia, Depressed Level of Consciousness
Adverse event resulted in: life threatening event
Suspect drug(s):
Avelox (Moxifloxacin)
Other drugs received by patient: Mucodyne
Adverse event in 69 year old female receiving Avelox (Moxifloxacin)
Reported by a consumer/non-health professional from United States on 2007-07-16
Patient: 69 year old female, weighing 71.7 kg (157.7 pounds)
Adverse reactions / side effects: Asthma, Basedow's Disease, Blood Bilirubin Increased, Hypersensitivity, Pyrexia, Constipation, Abdominal Discomfort, Cardiac Valve Disease, Fatigue, Chest Pain, Oedema Peripheral, Electrolyte Imbalance, Heart Rate Irregular, Vomiting, Fluorosis, Nausea, Blood Phosphorus Increased, Chromaturia, Muscular Weakness, Cardiomyopathy, Exercise Tolerance Decreased, Tremor, Faeces Pale, Diarrhoea, Heart Rate Increased, Muscle Disorder
Adverse event resulted in: life threatening event, hospitalization, disablity
Suspect drug(s):
Avelox
Dosage: one tablet one per day po
Administration route: Oral
Indication: Pneumonia
Start date: 2007-06-26
End date: 2007-06-28
Ciprofloxacin HCL
Indication: Bronchitis
Start date: 2002-11-10
End date: 2002-11-20
Adverse event in 29 year old female receiving Avelox (Moxifloxacin)
Reported by a individual with unspecified qualification from United States on 2007-06-26
Patient: 29 year old female, weighing 99.8 kg (219.5 pounds)
Adverse reactions / side effects: Anaphylactic Shock
Adverse event resulted in: life threatening event
Suspect drug(s):
Avelox (Moxifloxacin)
Adverse event in 21 year old female receiving Avelox (Moxifloxacin)
Reported by a health professional (non-physician/pharmacist) from United States on 2007-06-21
Patient: 21 year old female
Adverse reactions / side effects: Anaphylactic Reaction, Disseminated Intravascular Coagulation, Hepatic Failure, Paralysis, Hypokalaemia, Cardio-Respiratory Arrest, Cyanosis, Pneumothorax, Brain Oedema, Brain Damage, Mucous Membrane Disorder, Dyspnoea, Anoxic Encephalopathy, Hyperglycaemia, Hypotension, Pseudomonal Bacteraemia, Apallic Syndrome, Grand MAL Convulsion, Staphylococcal Infection, Respiratory Failure, Respiratory Arrest, Depressed Level of Consciousness
Adverse event resulted in: life threatening event, hospitalization, disablity
Suspect drug(s):
Avelox (Moxifloxacin)
Other drugs received by patient: Ortho TRI-Cyclen; Rhinocort; Zomig; Sudafed 12 Hour; Advil; Tegretol; Neurontin
Adverse event in 44 year old male receiving Avelox (Moxifloxacin)
Reported by a physician from Hungary on 2007-05-10
Patient: 44 year old male, weighing 75.0 kg (165.0 pounds)
Adverse reactions / side effects: Sepsis, Meningitis Bacterial
Adverse event resulted in: death, life threatening event
Suspect drug(s):
Avelox (Moxifloxacin)
Other drugs received by patient: Ambroxol; Tavanic
Adverse event in 45 year old male receiving Avelox (Moxifloxacin)
Reported by a physician from United States on 2007-04-25
Patient: 45 year old male
Adverse reactions / side effects: Angioedema, Pharyngeal Oedema, Swelling Face, Cardiac Enzymes Increased, Respiratory Arrest, Electrocardiogram Q Wave Abnormal, Troponin Increased
Adverse event resulted in: life threatening event, hospitalization
Suspect drug(s):
Avelox (Moxifloxacin)
Adverse event in 46 year old female receiving Avelox (Moxifloxacin)
Reported by a health professional (non-physician/pharmacist) from United States on 2007-04-19
Patient: 46 year old female, weighing 65.8 kg (144.7 pounds)
Adverse reactions / side effects: Pruritus Generalised, Oral Discomfort, Pharyngeal Oedema, Dyspnoea, Throat Irritation, Dizziness, Oral Pruritus, Asthenia, Eye Pruritus
Adverse event resulted in: life threatening event, hospitalization
Suspect drug(s):
Avelox (Moxifloxacin)
Adverse event in 75 year old female receiving Avelox (Moxifloxacin)
Reported by a pharmacist from United States on 2007-04-17
Patient: 75 year old female
Adverse reactions / side effects: Death, Electrocardiogram QT Prolonged, Torsade DE Pointes, Unresponsive TO Stimuli, Sinus Tachycardia
Adverse event resulted in: death, life threatening event, hospitalization
Suspect drug(s):
Avelox (Moxifloxacin)
Other drugs received by patient: Diltiazem; Digoxin
Adverse event in 44 year old male receiving Avelox (Moxifloxacin)
Reported by a physician from Hungary on 2007-04-17
Patient: 44 year old male, weighing 75.0 kg (165.0 pounds)
Adverse reactions / side effects: Sepsis, Meningitis Bacterial
Adverse event resulted in: death, life threatening event
Suspect drug(s):
Avelox (Moxifloxacin)
Other drugs received by patient: Ambroxol; Tavanic
Adverse event in 79 year old female receiving Avelox (Moxifloxacin)
Reported by a pharmacist from Canada on 2007-04-17
Patient: 79 year old female, weighing 68.0 kg (149.6 pounds)
Adverse reactions / side effects: Hypoglycaemia
Adverse event resulted in: life threatening event
Suspect drug(s):
Avelox (Moxifloxacin)
Other drugs received by patient: Diamicron; Diamicron
Adverse event in 75 year old female receiving Avelox (Moxifloxacin)
Reported by a pharmacist from United States on 2007-04-04
Patient: 75 year old female
Adverse reactions / side effects: Death, Electrocardiogram QT Prolonged, Torsade DE Pointes, Unresponsive TO Stimuli, Sinus Tachycardia
Adverse event resulted in: death, life threatening event, hospitalization
Suspect drug(s):
Avelox (Moxifloxacin)
Other drugs received by patient: Diltiazem; Digoxin
Adverse event in 75 year old female receiving Avelox (Moxifloxacin)
Reported by a pharmacist from United States on 2007-03-30
Patient: 75 year old female
Adverse reactions / side effects: Death, Torsade DE Pointes, Unresponsive TO Stimuli, Sinus Tachycardia
Adverse event resulted in: death, life threatening event, hospitalization
Suspect drug(s):
Avelox (Moxifloxacin)
Other drugs received by patient: Diltiazem; Digoxin
Adverse event in 40 year old female receiving Avelox (Moxifloxacin)
Reported by a physician from United States on 2007-03-30
Patient: 40 year old female
Adverse reactions / side effects: Hepatic Function Abnormal, Hepatic Necrosis, Alanine Aminotransferase Increased, Hepatic Failure, Rash, Liver Disorder, Malaise, Yellow Skin, Hepatotoxicity, Aspartate Aminotransferase Increased
Adverse event resulted in: life threatening event, hospitalization
Suspect drug(s):
Avelox
Administration route: Oral
Indication: Ear Infection
Start date: 2006-06-01
End date: 2006-06-01
Zetia
Administration route: Oral
[therapy Unspecified]
Other drugs received by patient: [therapy Unspecified]
Adverse event in female receiving Avelox (Moxifloxacin)
Reported by a health professional (non-physician/pharmacist) from United States on 2007-03-29
Patient: female
Adverse reactions / side effects: Blood Creatine Phosphokinase Increased, Anaphylactic Reaction, Peripheral Vascular Disorder, Haemodialysis, Loss of Consciousness, Renal Failure, Limb Discomfort, Limb Injury, Dehydration, Poor Peripheral Circulation
Adverse event resulted in: life threatening event, hospitalization
Suspect drug(s):
Another Antibiotic (Nos)
Indication: Drug USE FOR Unknown Indication
Avelox
Administration route: Oral
Indication: Respiratory Tract Infection
Start date: 2006-12-01
End date: 2006-12-01
Adverse event in 50 year old female receiving Avelox (Moxifloxacin)
Reported by a individual with unspecified qualification from United States on 2007-03-27
Patient: 50 year old female, weighing 86.6 kg (190.6 pounds)
Adverse reactions / side effects: Anaphylactic Shock, Loss of Consciousness
Adverse event resulted in: life threatening event, hospitalization
Suspect drug(s):
Avelox (Moxifloxacin)
Adverse event in 66 year old female receiving Avelox (Moxifloxacin)
Reported by a physician from Japan on 2007-03-21
Patient: 66 year old female
Adverse reactions / side effects: Pneumonia
Adverse event resulted in: life threatening event, hospitalization
Suspect drug(s):
Avelox
Dosage: total daily dose: 400 mg unit dose: 400 mg
Administration route: Oral
Indication: Pneumonia
Start date: 2006-05-15
End date: 2006-05-17
Avelox
Dosage: total daily dose: 400 mg unit dose: 400 mg
Administration route: Oral
Start date: 2006-06-01
End date: 2006-06-12
Rheumatrex
Dosage: total daily dose: 8 mg
Administration route: Oral
Indication: Rheumatoid Arthritis
End date: 2006-05-15
Other drugs received by patient: Medrol; Dogmatyl; Gaslon N; Bisolvon; Mucodyne; Benet; Sucralfate; Ciprofloxacin; Unasyn; Dalacin; Erythrocin
Adverse event in 64 year old male receiving Avelox (Moxifloxacin)
Reported by a physician from United States on 2007-03-20
Patient: 64 year old male, weighing 146.0 kg (321.2 pounds)
Adverse reactions / side effects: Abdominal Pain, Dyspnoea, Vomiting, Wrong Technique in Drug Usage Process, Nausea, Drug Hypersensitivity, Urticaria, Rash
Adverse event resulted in: life threatening event
Suspect drug(s):
Avelox
Indication: Bronchitis
Januvia
Administration route: Oral
Indication: Diabetes Mellitus
Adverse event in 64 year old male receiving Avelox (Moxifloxacin)
Reported by a physician from United States on 2007-03-16
Patient: 64 year old male, weighing 146.0 kg (321.2 pounds)
Adverse reactions / side effects: Abdominal Pain, Dyspnoea, Vomiting, Wrong Technique in Drug Usage Process, Nausea, Drug Hypersensitivity, Urticaria, Rash
Adverse event resulted in: life threatening event
Suspect drug(s):
Avelox
Indication: Bronchitis
Januvia
Administration route: Oral
Indication: Diabetes Mellitus
Adverse event in 84 year old female receiving Avelox (Moxifloxacin)
Reported by a physician from Belgium on 2007-03-12
Patient: 84 year old female
Adverse reactions / side effects: Cardio-Respiratory Arrest, Anaphylactic Shock, Respiratory Tract Infection
Adverse event resulted in: death, life threatening event, hospitalization
Suspect drug(s):
Avelox (Moxifloxacin)
Other drugs received by patient: Diureticum (Unspecified); Antihypertensivum (Unspecified)
Adverse event in 74 year old female receiving Avelox (Moxifloxacin)
Reported by a consumer/non-health professional from United States on 2007-03-12
Patient: 74 year old female, weighing 78.5 kg (172.6 pounds)
Adverse reactions / side effects: Burning Sensation, Nerve Injury, Dyspnoea, Dysstasia, Skin Discolouration, Anaphylactic Reaction, Loss of Consciousness
Adverse event resulted in: life threatening event, disablity
Suspect drug(s):
Avelox
Dosage: 1 tablet-mg.? once a day by mouth
Administration route: Oral
Indication: Bronchitis
Start date: 2007-01-31
Avelox
Dosage: 1 tablet-mg.? once a day by mouth
Administration route: Oral
Indication: Pneumonia
Start date: 2007-01-31
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