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Avelox (Moxifloxacin) - Life Threatening Events - Suspected Cause - Side Effect Reports

 
 



Index of reports > Life Threatening Events (79)

Below is the selection of side effect reports (a.k.a. adverse event reports) related to Avelox (Moxifloxacin) life threatening events. The selected reports were submitted to the FDA during the sample period of about a year.

 Reports 1 - 30 of 79   Next >>

Possible Avelox side effects in 41 year old male

Reported by a consumer/non-health professional from Canada on 2012-08-23

Patient: 41 year old male, weighing 100.0 kg (220.0 pounds)

Reactions: Abdominal Pain, Vomiting, Arthralgia, Anaphylactic Reaction, Dizziness, Skin Burning Sensation, Hypoaesthesia, Loss of Consciousness

Adverse event resulted in: life threatening event

Drug(s) suspected as cause:
Avelox



Possible Avelox side effects in female

Reported by a physician from United States on 2012-08-23

Patient: female, weighing 59.0 kg (129.7 pounds)

Reactions: Incoherent, Tachycardia, Hypotension, Hyperhidrosis

Adverse event resulted in: life threatening event

Drug(s) suspected as cause:
Avelox
    Dosage: qd, po
    Administration route: Oral
    Indication: Upper Respiratory Tract Infection
    Start date: 2011-12-15

Avelox
    Dosage: qd, po
    Administration route: Oral
    Indication: Pyrexia
    Start date: 2011-12-15

Avelox
    Dosage: qd, po
    Administration route: Oral
    Indication: Cough
    Start date: 2011-12-15



Possible Avelox side effects in female

Reported by a consumer/non-health professional from United States on 2012-08-20

Patient: female, weighing 54.4 kg (119.7 pounds)

Reactions: Anxiety, Nightmare, Feeling Abnormal, Fall, Hallucination

Adverse event resulted in: life threatening event, hospitalization

Drug(s) suspected as cause:
Avelox

Other drugs received by patient: Ketorolac



Possible Avelox side effects in 29 year old female

Reported by a health professional (non-physician/pharmacist) from Switzerland on 2012-08-15

Patient: 29 year old female

Reactions: Agranulocytosis, Systemic Inflammatory Response Syndrome

Adverse event resulted in: life threatening event, hospitalization

Drug(s) suspected as cause:
Avelox
    Dosage: unk
    Administration route: Oral
    Start date: 2012-06-26
    End date: 2012-06-27

Avelox
    Dosage: unk
    Start date: 2012-07-03
    End date: 2012-07-04

Ciprofloxacin HCL
    Dosage: unk
    Administration route: Oral
    Start date: 2012-07-07
    End date: 2012-07-10

Mesalamine
    Dosage: daily dose 6 df
    Start date: 2012-06-28
    End date: 2012-07-10

Mesalamine
    Dosage: 500 mg, tid
    Administration route: Oral
    Indication: Crohn's Disease
    Start date: 2011-09-19

Novalgin
    Dosage: unk
    Administration route: Oral
    Start date: 2012-07-07
    End date: 2012-07-09

Other drugs received by patient: Levothyroxine Sodium



Possible Avelox side effects in 63 year old female

Reported by a consumer/non-health professional from Croatia (Local Name: Hrvatska) on 2012-07-25

Patient: 63 year old female

Reactions: LIP Swelling, Angioedema, Oropharyngeal Pain, Swollen Tongue

Adverse event resulted in: life threatening event

Drug(s) suspected as cause:
Avelox



Possible Avelox side effects in 74 year old female

Reported by a pharmacist from United States on 2012-07-19

Patient: 74 year old female, weighing 70.3 kg (154.7 pounds)

Reactions: Pneumonia, Unresponsive To Stimuli, Hypoglycaemia

Adverse event resulted in: life threatening event

Drug(s) suspected as cause:
Avelox
    Dosage: 400 mg daily po
    Indication: Hypoglycaemia
    Start date: 2011-03-02
    End date: 2011-03-02

Glyburide
    Dosage: 10 mg twice daily po
    Administration route: Oral
    Indication: Pneumonia
    Start date: 2011-03-02
    End date: 2011-03-02



Possible Avelox side effects in 62 year old male

Reported by a physician from Germany on 2012-07-03

Patient: 62 year old male

Reactions: Pruritus, Toxic Epidermal Necrolysis, Pyrexia, Nikolsky's Sign, Stevens-Johnson Syndrome, Blister

Adverse event resulted in: life threatening event, hospitalization

Drug(s) suspected as cause:
Acetylcysteine
    Dosage: 300 mg, 2x/day
    Administration route: Oral
    Indication: Mucous Membrane Disorder
    Start date: 2005-06-29
    End date: 2005-07-12

ALT-Insulin
    Dosage: df
    Indication: Blood Glucose
    Start date: 2005-07-03
    End date: 2005-07-03

Ambroxol
    Dosage: 14 gtt, 2x/day
    Administration route: Oral
    Indication: Mucous Membrane Disorder
    Start date: 2005-07-01
    End date: 2005-07-18

Avelox
    Indication: Chronic Obstructive Pulmonary Disease

Avelox
    Dosage: 400 mg, 1x/day
    Administration route: Oral
    Indication: Infection
    Start date: 2005-06-27
    End date: 2005-07-03

Berotec
    Dosage: 2-3 times weekly
    Indication: Chronic Obstructive Pulmonary Disease
    Start date: 2004-06-01

Bricanyl
    Dosage: 0.5 df, 2x/day
    Indication: Dyspnoea
    Start date: 2005-06-27
    End date: 2005-07-09

Calcium
    Dosage: 500 mg, 2x/day
    Administration route: Oral
    Indication: Osteoporosis
    Start date: 2005-07-15
    End date: 2005-07-18

Calcium Carbonate
    Dosage: 2 df, 1x/day
    Administration route: Oral
    Indication: Osteoporosis
    Start date: 2005-07-19

Clonidine Hydrochloride
    Dosage: 1.5 g, 1x/day
    Indication: Alcohol Withdrawal Syndrome
    Start date: 2005-06-28
    End date: 2005-06-30

Clonidine Hydrochloride
    Dosage: 1.5 g, 1x/day
    Start date: 2005-07-03
    End date: 2005-07-04

Clorazepate Dipotassium
    Dosage: 5 mg, 3x/day
    Administration route: Oral
    Start date: 2005-07-05
    End date: 2005-07-05

Clorazepate Dipotassium
    Dosage: 5 mg, 3x/day
    Administration route: Oral
    Indication: Sedation
    Start date: 2005-06-27
    End date: 2005-07-02

Delix Plus
    Dosage: 1 df, 1x/day
    Administration route: Oral
    Indication: Myocardial Ischaemia
    Start date: 2005-07-03

Digitoxin TAB
    Dosage: 0.1 mg, 1x/day
    Administration route: Oral
    Indication: Myocardial Ischaemia
    Start date: 2005-07-08

Distraneurin
    Dosage: 2.0 df, 3x/day
    Administration route: Oral
    Indication: Alcohol Withdrawal Syndrome
    Start date: 2005-06-30
    End date: 2005-07-03

Ergocalciferol
    Dosage: 1000 iu, 1x/day
    Administration route: Oral
    Indication: Osteoporosis
    Start date: 2005-07-18
    End date: 2005-07-18

Fluticasone Propionate
    Dosage: unk
    Start date: 2005-07-18

Foradil
    Dosage: 1 df, 2x/day
    Indication: Chronic Obstructive Pulmonary Disease
    Start date: 2005-06-29
    End date: 2005-07-18

Furosemide
    Dosage: 40 mg, 1x/day
    Administration route: Oral
    Start date: 2005-07-07

Haloperidol
    Dosage: 10 gtt, 1x/day
    Administration route: Oral
    Start date: 2005-07-03
    End date: 2005-07-03

Haloperidol
    Dosage: 10 gtt, 1x/day
    Administration route: Oral
    Indication: Sedation
    Start date: 2005-06-29
    End date: 2005-06-30

Heparin
    Dosage: 25000 iu, 1x/day
    Indication: Thrombosis
    Start date: 2005-06-27
    End date: 2005-07-09

Isoptin
    Dosage: 80 mg, 2x/day
    Administration route: Oral
    Indication: Arrhythmia
    Start date: 2005-07-09

Isoptin
    Dosage: 80 mg unknown frequency
    Administration route: Oral
    Indication: Atrial Fibrillation
    Start date: 2005-07-18

Junik
    Dosage: 1 df, 2x/day
    Indication: Chronic Obstructive Pulmonary Disease
    Start date: 2005-06-27
    End date: 2005-07-15

Kalinor-Brausetabletten
    Dosage: 1 df, 1x/day
    Administration route: Oral
    Indication: Hypokalaemia
    Start date: 2005-07-04
    End date: 2005-07-14

Marcumar
    Dosage: ^df^
    Administration route: Oral
    Indication: Atrial Fibrillation
    Start date: 2005-07-10

Nitroglycerin
    Dosage: 50 mg, 1x/day
    Indication: Essential Hypertension
    Start date: 2005-07-02
    End date: 2005-07-02

Norvasc
    Dosage: 5 mg, 1x/day
    Administration route: Oral
    Start date: 2005-07-04
    End date: 2005-07-09

Omeprazole
    Dosage: 20 mg, 1x/day, in the evening
    Administration route: Oral
    Indication: Gastric Disorder
    Start date: 2005-07-19

Oxazepam
    Dosage: ^df^
    Administration route: Oral
    Indication: Sedation
    Start date: 2005-07-08
    End date: 2005-07-08

Pantoprazole
    Dosage: 40 mg, 1x/day
    Administration route: Oral
    Indication: Prophylaxis Against Gastrointestinal Ulcer
    Start date: 2005-06-29
    End date: 2005-06-30

Pantoprazole
    Dosage: 40 mg, 1x/day
    Administration route: Oral
    Start date: 2005-07-03
    End date: 2005-07-18

Prednisolone
    Dosage: 15 mg, 1x/day
    Administration route: Oral
    Indication: Chronic Obstructive Pulmonary Disease
    Start date: 2005-07-16
    End date: 2005-07-18

Prednisolone
    Dosage: 100 mg, 1x/day
    Administration route: Oral
    Start date: 2005-07-21
    End date: 2005-07-21

Prednisone TAB
    Dosage: unknown
    Administration route: Oral
    Start date: 2005-07-19

Prednisone TAB
    Dosage: unknown
    Administration route: Oral
    Start date: 2005-07-07
    End date: 2005-07-15

Prednisone TAB
    Dosage: unknown
    Administration route: Oral
    Indication: Chronic Obstructive Pulmonary Disease
    Start date: 2005-06-28
    End date: 2005-07-05

Ramipril
    Dosage: ^df daily^
    Administration route: Oral
    Indication: Myocardial Ischaemia
    Start date: 2005-06-30
    End date: 2005-07-02

Salmeterol Xinafoate
    Dosage: unk
    Start date: 2005-07-18

Salutec
    Dosage: 5/25 daily
    Administration route: Oral
    Indication: Coronary Artery Disease
    Start date: 2005-07-03

Sodium Chloride
    Dosage: 1000 ml/day
    Indication: Hypovolaemia
    Start date: 2005-06-27
    End date: 2005-07-03

Spiriva
    Dosage: 1 df, 1x/day
    Indication: Chronic Obstructive Pulmonary Disease
    Start date: 2004-06-01

Theophylline
    Dosage: 200 - 600 mg
    Indication: Chronic Obstructive Pulmonary Disease
    Start date: 2005-06-27
    End date: 2005-06-30

Theophylline
    Dosage: 200 mg, unk
    Start date: 2005-07-21
    End date: 2005-07-21

Theophylline
    Dosage: 600 mg, 1x/day
    Administration route: Oral

Theophylline
    Dosage: 600 mg, 1x/day
    Administration route: Oral
    Start date: 2005-07-03
    End date: 2005-07-09

Theophylline
    Dosage: 200 mg, unk
    Start date: 2005-07-18
    End date: 2005-07-18

Verapamil
    Dosage: 80 mg - 240 mg daily
    Administration route: Oral
    Indication: Tachyarrhythmia
    Start date: 2005-07-18

Verapamil
    Dosage: 80 mg, 3x/day
    Administration route: Oral



Possible Avelox side effects in 62 year old male

Reported by a health professional (non-physician/pharmacist) from Germany on 2012-06-29

Patient: 62 year old male

Reactions: Pruritus, Toxic Epidermal Necrolysis, Pyrexia, Nikolsky's Sign, Stevens-Johnson Syndrome, Blister

Adverse event resulted in: life threatening event, hospitalization

Drug(s) suspected as cause:
Acetylcysteine
    Dosage: 600 mg, 1x/day
    Administration route: Oral
    Start date: 2005-06-29
    End date: 2005-07-12

Acetylcysteine
    Dosage: 300 mg, 2x/day
    Administration route: Oral
    Indication: Mucous Membrane Disorder
    Start date: 2005-06-29
    End date: 2005-07-12

ALT-Insulin
    Dosage: unk
    Indication: Blood Glucose
    Start date: 2005-07-03
    End date: 2005-07-03

Ambroxol
    Dosage: 14 gtt, 2x/day
    Administration route: Oral
    Indication: Mucous Membrane Disorder
    Start date: 2005-07-01
    End date: 2005-07-18

Ambroxol
    Indication: Evidence Based Treatment

Avelox
    Dosage: 400 mg, 1x/day
    Administration route: Oral
    Indication: Chronic Obstructive Pulmonary Disease
    Start date: 2005-06-27
    End date: 2005-07-03

Berotec
    Dosage: 2-3 times, weekly
    Indication: Chronic Obstructive Pulmonary Disease
    Start date: 2004-06-01

Bricanyl
    Dosage: 1 ampoule
    Indication: Dyspnoea
    Start date: 2005-06-27
    End date: 2005-07-09

Calcium
    Dosage: 500 mg, 2x/day
    Administration route: Oral
    Indication: Osteoporosis
    Start date: 2005-07-15
    End date: 2005-07-18

Calcium Carbonate
    Dosage: 2 df, 1x/day
    Administration route: Oral
    Indication: Osteoporosis
    Start date: 2005-07-19

Clonidine Hydrochloride
    Dosage: 1.5 mg, 1x/day
    Indication: Alcohol Withdrawal Syndrome
    Start date: 2005-06-28
    End date: 2005-06-30

Clonidine Hydrochloride
    Dosage: 1.5 mg, 1x/day
    Start date: 2005-07-03
    End date: 2005-07-04

Clorazepate Dipotassium
    Dosage: 5 mg, 3x/day + 10 mg at night
    Administration route: Oral
    Indication: Sedation
    Start date: 2005-06-27
    End date: 2005-07-02

Clorazepate Dipotassium
    Dosage: 5 mg, 3x/day + 10 mg at night
    Administration route: Oral
    Start date: 2005-07-05
    End date: 2005-07-05

Delix Plus
    Administration route: Oral
    Indication: Cardiac Disorder

Digitoxin TAB
    Dosage: 0.1 mg, 1x/day
    Administration route: Oral
    Indication: Cardiac Disorder
    Start date: 2005-07-08

Distraneurin
    Dosage: 2 df, 3x/day
    Administration route: Oral
    Indication: Alcohol Withdrawal Syndrome
    Start date: 2005-06-30
    End date: 2005-07-03

Ergocalciferol
    Dosage: 100 iu, 1x/day
    Administration route: Oral
    Indication: Osteoporosis
    Start date: 2005-07-18
    End date: 2005-07-18

Fluticasone Propionate / Salmeterol
    Indication: Chronic Obstructive Pulmonary Disease

Foradil
    Dosage: 2 df, 1x/day
    Indication: Chronic Obstructive Pulmonary Disease
    Start date: 2005-06-29
    End date: 2005-07-18

Furosemid
    Dosage: 40 mg, 1x/day
    Administration route: Oral
    Indication: Hypertension
    Start date: 2005-07-07

Haloperidol
    Dosage: 10 gtt, 1x/day
    Administration route: Oral
    Start date: 2005-07-03
    End date: 2005-07-03

Haloperidol
    Dosage: 10 gtt, 1x/day
    Administration route: Oral
    Indication: Sedation
    Start date: 2005-06-29
    End date: 2005-06-30

Heparin
    Dosage: 25000 iu, unk
    Indication: Prophylaxis
    Start date: 2005-06-27
    End date: 2005-07-09

Junik
    Dosage: 2 df, 1x/day
    Indication: Chronic Obstructive Pulmonary Disease
    Start date: 2005-06-27
    End date: 2005-07-15

Kalinor-Brausetabletten
    Dosage: 1 df, 1x/day
    Administration route: Oral
    Indication: Hypokalaemia
    Start date: 2005-07-04
    End date: 2005-07-14

Marcumar
    Dosage: unk
    Administration route: Oral
    Indication: Atrial Fibrillation
    Start date: 2005-07-10

Nitroglycerin
    Dosage: 50 mg, unk
    Indication: Hypertension
    Start date: 2005-07-02
    End date: 2005-07-02

Norvasc
    Dosage: 5 mg, 1x/day
    Administration route: Oral
    Indication: Cardiac Disorder
    Start date: 2005-07-04
    End date: 2005-07-09

Omeprazole
    Dosage: 20 mg, 1x/day in the evening
    Administration route: Oral
    Indication: Gastric Disorder
    Start date: 2005-07-19

Oxazepam
    Dosage: unk
    Administration route: Oral
    Indication: Sedation
    Start date: 2005-07-08
    End date: 2005-07-08

Pantoprazole
    Dosage: 40 mg, 1x/day
    Administration route: Oral
    Indication: Prophylaxis
    Start date: 2005-07-03
    End date: 2005-07-18

Pantoprazole
    Dosage: unk
    Administration route: Oral
    Start date: 2005-06-29
    End date: 2005-06-30

Prednisolone
    Dosage: 20 mg, 1x/day
    Administration route: Oral
    Indication: Chronic Obstructive Pulmonary Disease
    Start date: 2005-07-19

Prednisolone
    Dosage: 50 mg, 1x/day
    Administration route: Oral
    Start date: 2005-06-28
    End date: 2005-07-05

Prednisolone
    Dosage: 100 mg, 1x/day
    Administration route: Oral
    Start date: 2005-07-21
    End date: 2005-07-21

Prednisolone
    Dosage: 80 mg, 1x/day
    Administration route: Oral
    Start date: 2005-07-07
    End date: 2005-07-15

Prednisolone
    Dosage: 15 mg, 1x/day
    Administration route: Oral
    Indication: Chronic Obstructive Pulmonary Disease
    Start date: 2005-07-16
    End date: 2005-07-18

Prednisolone
    Dosage: 15 mg, 1x/day
    Administration route: Oral
    Start date: 2005-07-16
    End date: 2005-07-18

Prednisolone
    Dosage: 100 mg, 1x/day
    Administration route: Oral
    Start date: 2005-07-21
    End date: 2005-07-21

Prednisolone
    Dosage: 5 mg, unk
    Administration route: Oral

Ramipril
    Dosage: 1 df, 1x/day
    Administration route: Oral
    Indication: Coronary Artery Disease
    Start date: 2005-06-30
    End date: 2005-07-02

Ringer's
    Dosage: 1000 ml, 1x/day
    Indication: Fluid Replacement
    Start date: 2005-06-27
    End date: 2005-07-03

Ringer's
    Indication: Volume Blood Increased

Salutec
    Dosage: 5/25 daily
    Administration route: Oral
    Indication: Coronary Artery Disease
    Start date: 2005-07-03

Spiriva
    Dosage: 1 df, 1x/day
    Indication: Chronic Obstructive Pulmonary Disease
    Start date: 2004-06-01

Theophylline
    Dosage: 200 mg - 600 mg
    Start date: 2005-06-27
    End date: 2005-06-30

Theophylline
    Dosage: 600 mg, 1x/day
    Administration route: Oral
    Indication: Chronic Obstructive Pulmonary Disease
    Start date: 2005-07-03
    End date: 2005-07-09

Theophylline
    Dosage: 600 mg, unk

Theophylline
    Dosage: 200 mg, unk
    Start date: 2005-07-21
    End date: 2005-07-21

Theophylline
    Dosage: 200 mg, unk
    Start date: 2005-07-18
    End date: 2005-07-18

Verapamil HCL
    Dosage: 80 mg, 2x/day
    Administration route: Oral
    Indication: Atrial Fibrillation
    Start date: 2005-07-09

Verapamil Hydrochloride
    Dosage: 80 mg-240mg, daily
    Administration route: Oral
    Indication: Tachyarrhythmia
    Start date: 2005-07-18

Verapamil Hydrochloride
    Dosage: 80 mg, 3x/day
    Administration route: Oral



Possible Avelox side effects in male

Reported by a consumer/non-health professional from United States on 2012-06-26

Patient: male

Reactions: LIP Swelling, Eye Swelling, Anaphylactic Shock, Swollen Tongue

Adverse event resulted in: life threatening event

Drug(s) suspected as cause:
Avelox



Possible Avelox side effects in 29 year old female

Reported by a consumer/non-health professional from United States on 2012-06-20

Patient: 29 year old female

Reactions: Pharyngeal Oedema, Throat Tightness

Adverse event resulted in: life threatening event, hospitalization

Drug(s) suspected as cause:
Avelox



Possible Avelox side effects in 52 year old female

Reported by a individual with unspecified qualification from Canada on 2012-06-20

Patient: 52 year old female

Reactions: Drug Hypersensitivity, Crohn's Disease, Hypotension, Anaphylactic Shock, Drug Interaction, Cystitis, Disease Progression, Abdominal Discomfort, Dehydration, Incision Site Abscess, Dizziness, Abdominal Distension, Bladder Operation, White Blood Cell Count Increased

Adverse event resulted in: life threatening event, hospitalization

Drug(s) suspected as cause:
Amoxicillin
    Indication: Cystitis
    Start date: 2010-08-01

Avelox
    Indication: Cystitis
    Start date: 2010-08-01

Codeine
    Indication: Product Used FOR Unknown Indication
    Start date: 2010-08-01

Cotrim
    Indication: Cystitis

Remicade
    Dosage: 1 every 8 week(s)
    Indication: Crohn's Disease
    Start date: 2009-07-01

Remicade

Remicade
    Start date: 2010-09-13

Remicade
    Start date: 2010-09-13

Remicade
    Dosage: 1 every 8 week(s)

Other drugs received by patient possibly interacting with the suspect drug:
Macrobid
    Indication: Crohn's Disease
    Start date: 2010-08-01



Possible Avelox side effects in 90 year old male

Reported by a pharmacist from Canada on 2012-06-14

Patient: 90 year old male

Reactions: Confusional State, Cognitive Disorder

Adverse event resulted in: life threatening event

Drug(s) suspected as cause:
Avelox
    Dosage: 400 mg, qd
    Administration route: Oral
    Indication: Localised Infection
    Start date: 2012-03-20
    End date: 2012-05-03

Avelox
    Indication: Osteomyelitis

Other drugs received by patient: Antibiotics; Antibiotics



Possible Avelox side effects in female

Reported by a pharmacist from United States on 2012-06-08

Patient: female

Reactions: Anaphylactic Reaction

Adverse event resulted in: life threatening event

Drug(s) suspected as cause:
Avelox



Possible Avelox side effects in 81 year old male

Reported by a individual with unspecified qualification from United States on 2012-05-30

Patient: 81 year old male, weighing 69.9 kg (153.7 pounds)

Reactions: Dyspnoea, Clostridium Difficile Colitis, Hepatic Failure, Pyrexia, Oropharyngeal Pain, Aggression, Mental Impairment, Anxiety, Renal Failure, Mood Altered, Oral Candidiasis, Insomnia, Asthenia

Adverse event resulted in: life threatening event, hospitalization

Drug(s) suspected as cause:
Avelox



Possible Avelox side effects in female

Reported by a individual with unspecified qualification from United States on 2012-05-29

Patient: female, weighing 63.5 kg (139.7 pounds)

Reactions: Abdominal Pain, Movement Disorder, Dyspnoea, Paraesthesia Oral, Wheezing, Abasia, Muscular Weakness, Disorientation, Hyperhidrosis, Diarrhoea, Heart Rate Increased, Obstructive Airways Disorder, Blood Pressure Decreased, Oxygen Saturation Decreased

Adverse event resulted in: life threatening event, hospitalization

Drug(s) suspected as cause:
Avelox



Possible Avelox side effects in

Reported by a health professional (non-physician/pharmacist) from United States on 2012-05-29

Patient:

Reactions: Anaphylactic Reaction

Adverse event resulted in: life threatening event, hospitalization

Drug(s) suspected as cause:
Avelox



Possible Avelox side effects in 53 year old male

Reported by a health professional (non-physician/pharmacist) from Germany on 2012-05-29

Patient: 53 year old male, weighing 60.0 kg (132.0 pounds)

Reactions: Pneumonia, Tachyarrhythmia, Cardiovascular Insufficiency, Lactic Acidosis, Obliterative Bronchiolitis, Multi-Organ Failure, Renal Failure, Sepsis, Acute Hepatic Failure, Increased Bronchial Secretion, Shock

Adverse event resulted in: life threatening event, hospitalization

Drug(s) suspected as cause:
Avelox

Other drugs received by patient: Linezolid; Methadone HCL; Benzodiazepine



Possible Avelox side effects in 36 year old male

Reported by a physician from Austria on 2012-05-24

Patient: 36 year old male, weighing 110.0 kg (242.0 pounds)

Reactions: Hepatorenal Syndrome, Hepatic Failure

Adverse event resulted in: life threatening event

Drug(s) suspected as cause:
Avelox

Other drugs received by patient: Oxazepam; Keppra



Possible Avelox side effects in 67 year old male

Reported by a pharmacist from Canada on 2012-05-23

Patient: 67 year old male, weighing 105.0 kg (231.0 pounds)

Reactions: Mechanical Ventilation, Acquired Epidermolysis Bullosa, Hepatic Failure, Haematemesis, Liver Transplant, Malaise, Mallory-Weiss Syndrome, Depressed Level of Consciousness, Dermatitis Bullous, Pemphigoid, Renal Failure Acute

Adverse event resulted in: life threatening event, hospitalization

Drug(s) suspected as cause:
Avelox
    Dosage: 400 mg, qd
    Administration route: Oral
    Indication: Pneumonia
    Start date: 2011-09-12
    End date: 2011-09-22

Avelox
    Dosage: 400 mg, qd
    Administration route: Oral
    Start date: 2011-11-02
    End date: 2011-11-03

Other drugs received by patient: Sildenafil



Possible Avelox side effects in female

Reported by a health professional (non-physician/pharmacist) from United States on 2012-05-23

Patient: female

Reactions: Burning Sensation, Abdominal Pain, Urticaria, Throat Tightness, Erythema

Adverse event resulted in: life threatening event, hospitalization

Drug(s) suspected as cause:
Avelox



Possible Avelox side effects in 23 year old female

Reported by a health professional (non-physician/pharmacist) from Canada on 2012-05-22

Patient: 23 year old female

Reactions: Lymphadenopathy, Hepatic Necrosis, Hepatitis Acute, Hypotension, Hepatic Failure, Toxic Epidermal Necrolysis, Cholelithiasis, Renal Failure Acute

Adverse event resulted in: death, life threatening event, hospitalization

Drug(s) suspected as cause:
Avelox

Other drugs received by patient: Alesse



Possible Avelox side effects in 66 year old female

Reported by a physician from United States on 2012-05-22

Patient: 66 year old female

Reactions: Fatigue, Dyspnoea Exertional, Aphasia, Anaemia, Thrombotic Thrombocytopenic Purpura, Thrombocytopenia, Lethargy

Adverse event resulted in: life threatening event, hospitalization

Drug(s) suspected as cause:
Avelox
    Dosage: unk, bid
    Administration route: Oral
    Start date: 2011-01-01

Avelox
    Dosage: unk
    Indication: Sinusitis

Other drugs received by patient: Aspirin; Synthroid; Hydrochlorothiazide; Telmisartan; Fluticasone Furoate; Omeprazole



Possible Avelox side effects in

Reported by a health professional (non-physician/pharmacist) from Canada on 2012-05-21

Patient:

Reactions: Anaphylactic Shock, Drug Dispensing Error

Adverse event resulted in: life threatening event

Drug(s) suspected as cause:
Avelox



Possible Avelox side effects in 53 year old male

Reported by a health professional (non-physician/pharmacist) from Germany on 2012-05-16

Patient: 53 year old male, weighing 60.0 kg (132.0 pounds)

Reactions: Multi-Organ Failure, Acute Hepatic Failure, Lactic Acidosis, Shock

Adverse event resulted in: life threatening event, hospitalization

Drug(s) suspected as cause:
Avelox

Other drugs received by patient: Methadone HCL; Benzodiazepine



Possible Avelox side effects in 37 year old male

Reported by a physician from United States on 2012-05-14

Patient: 37 year old male, weighing 82.0 kg (180.4 pounds)

Reactions: Pruritus, Chest Discomfort, Respiratory Failure, Anaphylactic Reaction

Adverse event resulted in: life threatening event, hospitalization

Drug(s) suspected as cause:
Avelox



Possible Avelox side effects in 37 year old male

Reported by a physician from United States on 2012-05-14

Patient: 37 year old male, weighing 82.0 kg (180.4 pounds)

Reactions: Chest Discomfort, Pruritus, Respiratory Failure, Anaphylactic Reaction

Adverse event resulted in: life threatening event, hospitalization

Drug(s) suspected as cause:
Avelox



Possible Avelox side effects in 53 year old male

Reported by a health professional (non-physician/pharmacist) from Germany on 2012-04-23

Patient: 53 year old male, weighing 60.0 kg (132.0 pounds)

Reactions: Multi-Organ Failure, Acute Hepatic Failure, Lactic Acidosis

Adverse event resulted in: life threatening event, hospitalization

Drug(s) suspected as cause:
Avelox

Other drugs received by patient: Benzodiazepine; Methadone HCL



Possible Avelox side effects in female

Reported by a health professional (non-physician/pharmacist) from United States on 2012-04-20

Patient: female

Reactions: Anaphylactic Shock, Rash

Adverse event resulted in: death, life threatening event, hospitalization, disablity

Drug(s) suspected as cause:
Avelox

Other drugs received by patient: Propranolol



Possible Avelox side effects in female

Reported by a consumer/non-health professional from United States on 2012-04-18

Patient: female

Reactions: Angioedema, Drug Ineffective

Adverse event resulted in: life threatening event, disablity

Drug(s) suspected as cause:
Avelox



Possible Avelox side effects in 67 year old male

Reported by a pharmacist from Canada on 2012-04-17

Patient: 67 year old male, weighing 105.0 kg (231.0 pounds)

Reactions: Mechanical Ventilation, Acquired Epidermolysis Bullosa, Hepatic Failure, Haematemesis, Liver Transplant, Mallory-Weiss Syndrome, Malaise, Depressed Level of Consciousness, Dermatitis Bullous, Pemphigoid, Renal Failure Acute

Adverse event resulted in: life threatening event, hospitalization

Drug(s) suspected as cause:
Avelox
    Dosage: 400 mg, qd
    Administration route: Oral

Avelox
    Dosage: 400 mg, qd
    Administration route: Oral

Other drugs received by patient: Sildenafil



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