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Index of reports
> Cases resulting in hospitalization (202)
Below is the selection of adverse event reports related to Avelox (Moxifloxacin) that includes cases resulting in hospitalization.
Reports 1 - 25 of 202 Next >>
Adverse event in 82 year old female receiving Avelox (Moxifloxacin)
Reported by a physician from Japan on 2007-10-30
Patient: 82 year old female
Adverse reactions / side effects: Anaphylactoid Reaction, Petechiae, Rash
Adverse event resulted in: hospitalization
Suspect drug(s):
Avelox (Moxifloxacin)
Other drugs received by patient: Doxazosin Mesylate; Aspirin; Sennoside; Norvasc; Nitroderm; Omeprazole
Adverse event in 50 year old female receiving Avelox (Moxifloxacin)
Reported by a physician from United States on 2007-10-26
Patient: 50 year old female
Adverse reactions / side effects: Abdominal Pain, Hypotension, Chills, Hyperhidrosis
Adverse event resulted in: hospitalization
Suspect drug(s):
Avelox (Moxifloxacin)
Adverse event in 82 year old female receiving Avelox (Moxifloxacin)
Reported by a physician from Japan on 2007-10-25
Patient: 82 year old female
Adverse reactions / side effects: Petechiae, Rash
Adverse event resulted in: hospitalization
Suspect drug(s):
Avelox (Moxifloxacin)
Other drugs received by patient: Doxazosin Mesylate; Aspirin; Sennoside; Norvasc; Nitroderm; Omeprazole
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 male receiving Avelox (Moxifloxacin)
Reported by a physician from Japan on 2007-10-22
Patient: male
Adverse reactions / side effects: Interstitial Lung Disease
Adverse event resulted in: hospitalization
Suspect drug(s):
Avelox
Dosage: unit dose: 400 mg
Administration route: Oral
Indication: Pneumonia
Kakkon-TO
Administration route: Oral
Indication: Nasopharyngitis
Meiact
Administration route: Oral
Indication: Nasopharyngitis
PL
Administration route: Oral
Indication: Nasopharyngitis
Adverse event in male receiving Avelox (Moxifloxacin)
Reported by a physician from United States on 2007-10-19
Patient: male
Adverse reactions / side effects: Skin Ulcer
Adverse event resulted in: hospitalization
Suspect drug(s):
Avelox (Moxifloxacin)
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 18 year old male receiving Avelox (Moxifloxacin)
Reported by a physician from Norway on 2007-10-16
Patient: 18 year old male
Adverse reactions / side effects: Blood Creatine Phosphokinase Increased, Rhabdomyolysis, Alanine Aminotransferase Increased, Aspartate Aminotransferase Increased
Adverse event resulted in: hospitalization
Suspect drug(s):
Avelox
Indication: Infection
Emselex Extended Release
Dosage: 7.5 mg/d
Administration route: Oral
Indication: Prostatitis
Other drugs received by patient: Norfloxacin; Antiasthmatics
Adverse event in 44 year old female receiving Avelox (Moxifloxacin)
Reported by a health professional (non-physician/pharmacist) from United States on 2007-10-16
Patient: 44 year old female, weighing 91.0 kg (200.2 pounds)
Adverse reactions / side effects: Incoherent, Dizziness, Muscle Twitching, Ill-Defined Disorder
Adverse event resulted in: hospitalization
Suspect drug(s):
Avelox (Moxifloxacin)
Adverse event in 32 year old female receiving Avelox (Moxifloxacin)
Reported by a health professional (non-physician/pharmacist) from United States on 2007-10-16
Patient: 32 year old female, weighing 57.0 kg (125.4 pounds)
Adverse reactions / side effects: Anxiety, Neuropathy, Fatigue, Palpitations, Pain, Tendonitis, Muscle Spasms
Adverse event resulted in: hospitalization
Suspect drug(s):
Antibiotic (Nos)
Avelox
Dosage: total daily dose: 200 mg unit dose: 400 mg
Administration route: Oral
Indication: Drug USE FOR Unknown Indication
Start date: 2007-04-23
Avelox
Dosage: total daily dose: 200 mg unit dose: 400 mg
Administration route: Oral
Start date: 2007-04-24
Oral Steroids (Nos)
Indication: Sinusitis
Adverse event in 38 year old female receiving Avelox (Moxifloxacin)
Reported by a individual with unspecified qualification from United States on 2007-10-12
Patient: 38 year old female, weighing 54.4 kg (119.7 pounds)
Adverse reactions / side effects: Panic Attack, Visual Disturbance, Insomnia, Dizziness, Tremor
Adverse event resulted in: hospitalization
Suspect drug(s):
Avelox
Dosage: 10 once a day po
Administration route: Oral
Indication: Sinusitis
Start date: 2007-10-10
End date: 2007-10-10
Levaquin
Dosage: 10 once a day po
Administration route: Oral
Indication: Sinusitis
Start date: 2007-10-03
End date: 2007-10-09
Adverse event in 95 year old female receiving Avelox (Moxifloxacin)
Reported by a pharmacist from United States on 2007-10-10
Patient: 95 year old female
Adverse reactions / side effects: Hypotension, Oxygen Saturation Decreased
Adverse event resulted in: hospitalization
Suspect drug(s):
Avelox (Moxifloxacin)
Other drugs received by patient: Diovan; Fosamax; Paroxetine; Tylenol (Caplet); Oscal+vit D; Multi-Vitamin
Adverse event in 21 year old female receiving Avelox (Moxifloxacin)
Reported by a physician from United States on 2007-10-10
Patient: 21 year old female
Adverse reactions / side effects: Blood Alkaline Phosphatase Increased, Vomiting, Nausea, Alanine Aminotransferase Increased, Pyrexia, Rash, Hepatitis, White Blood Cell Count Abnormal, Platelet Count Abnormal, Aspartate Aminotransferase Increased, Dehydration, Thrombocytopenia, Leukopenia
Adverse event resulted in: hospitalization
Suspect drug(s):
Avelox (Moxifloxacin)
Other drugs received by patient: Doxycycline
Adverse event in 42 year old female receiving Avelox (Moxifloxacin)
Reported by a health professional (non-physician/pharmacist) from United States on 2007-10-10
Patient: 42 year old female, weighing 67.6 kg (148.7 pounds)
Adverse reactions / side effects: Anxiety, Palpitations, Adverse Drug Reaction, Hypoaesthesia Facial, Dizziness, Hypoaesthesia, Paraesthesia
Adverse event resulted in: hospitalization
Suspect drug(s):
Avelox
Indication: Bronchitis
Start date: 2007-09-27
End date: 2007-09-28
Avelox
Indication: Sinusitis
Start date: 2007-09-27
End date: 2007-09-28
Adverse event in 65 year old male receiving Avelox (Moxifloxacin)
Reported by a pharmacist from United States on 2007-10-05
Patient: 65 year old male, weighing 90.0 kg (198.0 pounds)
Adverse reactions / side effects: Dyspnoea, Nausea, Urticaria, Presyncope, Hypotension, Chest Pain, Pyrexia
Adverse event resulted in: hospitalization
Suspect drug(s):
Avelox (Moxifloxacin)
Adverse event in 83 year old male receiving Avelox (Moxifloxacin)
Reported by a health professional (non-physician/pharmacist) from United States on 2007-10-05
Patient: 83 year old male
Adverse reactions / side effects: Jaundice, Abdominal Pain, Vomiting, Dyspnoea, Hypotension, Coma, Anaemia Haemolytic Autoimmune, Haemoglobin Decreased, Laboratory Test Abnormal, Bradycardia, Cardiac Arrest, Sinus Tachycardia, Oxygen Saturation Decreased
Adverse event resulted in: death, hospitalization
Suspect drug(s):
Avelox
Administration route: Oral
Indication: Pneumonia
Start date: 2007-08-02
End date: 2007-08-06
Rocephin
Start date: 2007-08-02
Tylenol (Caplet)
Start date: 2007-08-02
Other drugs received by patient: Lisinopril; Allopurinol
Adverse event in 83 year old male receiving Avelox (Moxifloxacin)
Reported by a health professional (non-physician/pharmacist) from United States on 2007-10-04
Patient: 83 year old male
Adverse reactions / side effects: Jaundice, Abdominal Pain, Vomiting, Dyspnoea, Hypotension, Coma, Anaemia Haemolytic Autoimmune, Haemoglobin Decreased, Laboratory Test Abnormal, Bradycardia, Cardiac Arrest, Sinus Tachycardia, Oxygen Saturation Decreased
Adverse event resulted in: death, hospitalization
Suspect drug(s):
Avelox
Administration route: Oral
Indication: Pneumonia
Start date: 2007-08-02
End date: 2007-08-06
Rocephin
Start date: 2007-08-02
Tylenol (Caplet)
Start date: 2007-08-02
Other drugs received by patient: Lisinopril; Allopurinol
Adverse event in female receiving Avelox (Moxifloxacin)
Reported by a physician from United States on 2007-10-02
Patient: female
Adverse reactions / side effects: Rectal Haemorrhage
Adverse event resulted in: hospitalization
Suspect drug(s):
Avelox (Moxifloxacin)
Adverse event in 62 year old female receiving Avelox (Moxifloxacin)
Reported by a physician from Brazil on 2007-10-01
Patient: 62 year old female
Adverse reactions / side effects: Delirium
Adverse event resulted in: hospitalization
Suspect drug(s):
Avelox (Moxifloxacin)
Adverse event in 83 year old male receiving Avelox (Moxifloxacin)
Reported by a individual with unspecified qualification from Germany on 2007-07-31
Patient: 83 year old male, weighing 170.0 kg (374.0 pounds)
Adverse reactions / side effects: Necrosis, LEG Amputation, Staphylococcal Sepsis, Abscess Bacterial
Adverse event resulted in: death, hospitalization
Suspect drug(s):
Avelox
Indication: Diabetic Foot Infection
Avelox
Administration route: Oral
Other drugs received by patient: Aspirin; Ramipril; Nebilet; Allopurinol; Nexium; Simvastatin
Adverse event in 85 year old female receiving Avelox (Moxifloxacin)
Reported by a physician from Germany on 2007-07-31
Patient: 85 year old female
Adverse reactions / side effects: Abdominal Pain, Ileus, Sepsis, Pseudomembranous Colitis, Osteolysis
Adverse event resulted in: death, hospitalization
Suspect drug(s):
Avelox (Moxifloxacin)
Other drugs received by patient: Spiriva; Symbicort; Arlevert; Omeprazole; Tramadol HCL; Ibuprofen; Novalgin; Amitriptyline HCL
Adverse event in 85 year old male receiving Avelox (Moxifloxacin)
Reported by a pharmacist from United States on 2007-07-27
Patient: 85 year old male, weighing 83.9 kg (184.6 pounds)
Adverse reactions / side effects: Myasthenia Gravis, Dyspnoea, Condition Aggravated
Adverse event resulted in: hospitalization
Suspect drug(s):
Avelox (Moxifloxacin)
Adverse event in receiving Avelox (Moxifloxacin)
Reported by a physician from United States on 2007-07-25
Patient:
Adverse reactions / side effects: Drug Interaction
Adverse event resulted in: hospitalization
Suspect drug(s):
Avelox (Moxifloxacin)
Other drugs received by patient possibly interacting with the suspect drug:
Quinapril
Adverse event in 44 year old female receiving Avelox (Moxifloxacin)
Reported by a health professional (non-physician/pharmacist) from United States on 2007-07-25
Patient: 44 year old female, weighing 91.0 kg (200.2 pounds)
Adverse reactions / side effects: Incoherent, Dizziness, Muscle Twitching, Ill-Defined Disorder
Adverse event resulted in: hospitalization
Suspect drug(s):
Avelox (Moxifloxacin)
Adverse event in 32 year old female receiving Avelox (Moxifloxacin)
Reported by a health professional (non-physician/pharmacist) from United States on 2007-07-25
Patient: 32 year old female, weighing 57.0 kg (125.4 pounds)
Adverse reactions / side effects: Anxiety, Neuropathy, Fatigue, Palpitations, Pain, Tendonitis, Muscle Spasms
Adverse event resulted in: hospitalization
Suspect drug(s):
Antibiotic (Nos)
Avelox
Dosage: total daily dose: 200 mg unit dose: 400 mg
Administration route: Oral
Indication: Drug USE FOR Unknown Indication
Start date: 2007-04-23
Avelox
Dosage: total daily dose: 200 mg unit dose: 400 mg
Administration route: Oral
Start date: 2007-04-24
Oral Steroids (Nos)
Indication: Sinusitis
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