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Avelox (Moxifloxacin) - Adverse Event Reports - All Cases - Nausea

 



Index of reports > All cases (548) > Cases with Nausea (37)

Below is the selection of adverse event reports related to Avelox (Moxifloxacin) that includes all cases where reactions include nausea.

 Reports 1 - 25 of 37   Next >>

Adverse event in 33 year old male receiving Avelox (Moxifloxacin)

Reported by a consumer/non-health professional from United States on 2007-10-17

Patient: 33 year old male, weighing 95.3 kg (209.6 pounds)

Adverse reactions / side effects: Back Pain, Chest Discomfort, Pruritus, Nausea, Stomach Discomfort, Headache, Paraesthesia, Anxiety, Diarrhoea, Depression

Suspect drug(s):
Avelox (Moxifloxacin)



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 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 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 39 year old female receiving Avelox (Moxifloxacin)

Reported by a physician from Japan on 2007-07-10

Patient: 39 year old female, weighing 48.0 kg (105.6 pounds)

Adverse reactions / side effects: Pneumonia, Nausea, Dizziness

Suspect drug(s):
Avelox (Moxifloxacin)

Other drugs received by patient: Brocin Codeine; Mucodyne; Mucosta; Zithromac; Zithromac; Clarithromycin; Clarithromycin; Dasen; Dasen; Transamin; Voltaren; Asverin; Asverin; Asverin



Adverse event in 40 year old female receiving Avelox (Moxifloxacin)

Reported by a individual with unspecified qualification from United States on 2007-07-05

Patient: 40 year old female, weighing 83.9 kg (184.6 pounds)

Adverse reactions / side effects: Confusional State, Bone Pain, Headache, Myalgia, Fatigue, Neck Pain, Chest Pain, Dizziness, Depression, Panic Reaction, Muscle Spasms, Back Pain, Restlessness, Nausea, Drug Hypersensitivity, Muscular Weakness, Facial Pain, Burning Sensation, Anxiety, Visual Disturbance, Arthralgia, Insomnia, Ear Pain, Neuralgia

Suspect drug(s):
Avelox (Moxifloxacin)



Adverse event in 39 year old female receiving Avelox (Moxifloxacin)

Reported by a physician from Japan on 2007-06-27

Patient: 39 year old female, weighing 48.0 kg (105.6 pounds)

Adverse reactions / side effects: Pneumonia, Nausea, Dizziness

Suspect drug(s):
Avelox (Moxifloxacin)

Other drugs received by patient: Brocin Codeine; Mucodyne; Mucosta; Zithromac; Zithromac; Clarithromycin; Clarithromycin; Dasen; Dasen; Transamin; Voltaren; Asverin; Asverin; Asverin



Adverse event in female receiving Avelox (Moxifloxacin)

Reported by a consumer/non-health professional from United States on 2007-06-25

Patient: female, weighing 72.6 kg (159.7 pounds)

Adverse reactions / side effects: Blood Pressure Increased, Nausea, Pain in Extremity, Tendon Rupture, Pain, Hypoaesthesia, Paraesthesia, Malaise, Arthralgia, Joint Swelling, Feeling Jittery, Heart Rate Increased, Dizziness, Asthenia, Nervousness

Suspect drug(s):
Avelox
    Dosage: 400 mg 1 x day oral
    Administration route: Oral
    Indication: Sinusitis
    Start date: 2007-03-06

Avelox
    Dosage: 400 mg 1 x day oral
    Administration route: Oral
    Indication: Sinusitis
    Start date: 2007-06-01



Adverse event in 54 year old female receiving Avelox (Moxifloxacin)

Reported by a physician from United States on 2007-06-19

Patient: 54 year old female, weighing 64.0 kg (140.8 pounds)

Adverse reactions / side effects: Tinnitus, Malaise, Nausea, Insomnia, Ear Pain, Deafness Neurosensory, Disturbance in Attention

Adverse event resulted in: disablity

Suspect drug(s):
Avelox (Moxifloxacin)

Other drugs received by patient: Diazepam



Adverse event in 39 year old female receiving Avelox (Moxifloxacin)

Reported by a health professional (non-physician/pharmacist) from United States on 2007-06-14

Patient: 39 year old female, weighing 55.0 kg (121.0 pounds)

Adverse reactions / side effects: Abdominal Pain, Hepatomegaly, Hepatotoxicity, Nausea, Liver Function Test Abnormal, Chills, Pyrexia, Hyperhidrosis, Decreased Appetite

Adverse event resulted in: hospitalization

Suspect drug(s):
Avelox
    Administration route: Oral
    Indication: Sinusitis
    Start date: 2007-04-03

Gonal-F
    Indication: Infertility
    Start date: 2007-03-05
    End date: 2007-03-16

Other drugs received by patient: Crinone



Adverse event in 56 year old female receiving Avelox (Moxifloxacin)

Reported by a consumer/non-health professional from United States on 2007-06-11

Patient: 56 year old female, weighing 78.0 kg (171.6 pounds)

Adverse reactions / side effects: Nausea, Pyrexia, Apparent Life Threatening Event, Hepatic Enzyme Increased

Adverse event resulted in: hospitalization

Suspect drug(s):
Avelox (Moxifloxacin)



Adverse event in 39 year old female receiving Avelox (Moxifloxacin)

Reported by a physician from Japan on 2007-06-11

Patient: 39 year old female

Adverse reactions / side effects: Pneumonia, Nausea

Suspect drug(s):
Avelox (Moxifloxacin)

Other drugs received by patient: Brocin; Mucodyne



Adverse event in 34 year old male receiving Avelox (Moxifloxacin)

Reported by a consumer/non-health professional from United States on 2007-06-07

Patient: 34 year old male, weighing 95.3 kg (209.6 pounds)

Adverse reactions / side effects: Nausea, Skin Burning Sensation, Hypoaesthesia, Hyperhidrosis, Anxiety, Eye Haemorrhage, Diarrhoea, Chest Pain, Ocular Hyperaemia, Heart Rate Increased

Adverse event resulted in: hospitalization

Suspect drug(s):
Avelox (Moxifloxacin)



Adverse event in 60 year old male receiving Avelox (Moxifloxacin)

Reported by a individual with unspecified qualification from Croatia (Local Name: Hrvatska) on 2007-05-30

Patient: 60 year old male, weighing 80.0 kg (176.0 pounds)

Adverse reactions / side effects: Vomiting, Ileus, Nausea

Suspect drug(s):
Avelox (Moxifloxacin)

Other drugs received by patient: Seretide; Tramadol HCL



Adverse event in female receiving Avelox (Moxifloxacin)

Reported by a health professional (non-physician/pharmacist) from United States on 2007-05-17

Patient: female

Adverse reactions / side effects: Incoherent, Syncope, Vomiting, Nausea, Adverse Drug Reaction, Dizziness, Loss of Consciousness

Adverse event resulted in: hospitalization

Suspect drug(s):
Avelox
    Dosage: 400 mg 1 tab po
    Administration route: Oral
    Indication: Bronchitis
    Start date: 2007-04-07

Avelox
    Dosage: 400 mg 1 tab po
    Administration route: Oral
    Indication: Sinusitis
    Start date: 2007-04-07



Adverse event in 39 year old female receiving Avelox (Moxifloxacin)

Reported by a health professional (non-physician/pharmacist) from United States on 2007-05-17

Patient: 39 year old female, weighing 55.0 kg (121.0 pounds)

Adverse reactions / side effects: Abdominal Pain, Hepatotoxicity, Nausea, Liver Function Test Abnormal, Chills, Liver Tenderness, Pyrexia, Hyperhidrosis, Decreased Appetite

Adverse event resulted in: hospitalization

Suspect drug(s):
Avelox
    Administration route: Oral
    Indication: Sinusitis
    Start date: 2007-04-03

Gonal-F
    Indication: Infertility
    Start date: 2007-03-05
    End date: 2007-03-16

Other drugs received by patient: Crinone



Adverse event in 49 year old male receiving Avelox (Moxifloxacin)

Reported by a health professional (non-physician/pharmacist) from United States on 2007-05-10

Patient: 49 year old male

Adverse reactions / side effects: Jaundice, Blood Bilirubin Increased, Blood Alkaline Phosphatase Increased, Autoimmune Hepatitis, Nausea, Alanine Aminotransferase Increased, Urticaria Generalised, Blood Albumin Increased, Dyspepsia, Aspartate Aminotransferase Increased, Bilirubin Conjugated Increased

Adverse event resulted in: hospitalization

Suspect drug(s):
Avelox (Moxifloxacin)

Other drugs received by patient: Avonex; Crestor; Zanaflex; Amoxicillin; Hydrocodone; Zanaflex; Crestor; Osteo BI-Flex; Ibuprofen; Tylenol; Prednisone TAB



Adverse event in 49 year old male receiving Avelox (Moxifloxacin)

Reported by a health professional (non-physician/pharmacist) from United States on 2007-05-09

Patient: 49 year old male

Adverse reactions / side effects: Jaundice, Blood Bilirubin Increased, Blood Alkaline Phosphatase Increased, Autoimmune Hepatitis, Nausea, Alanine Aminotransferase Increased, Urticaria Generalised, Blood Albumin Increased, Dyspepsia, Aspartate Aminotransferase Increased, Bilirubin Conjugated Increased

Adverse event resulted in: hospitalization

Suspect drug(s):
Avelox (Moxifloxacin)

Other drugs received by patient: Avonex; Crestor; Zanaflex; Amoxicillin; Hydrocodone; Zanaflex; Crestor; Osteo BI-Flex; Ibuprofen; Tylenol; Prednisone TAB



Adverse event in 39 year old female receiving Avelox (Moxifloxacin)

Reported by a health professional (non-physician/pharmacist) from United States on 2007-05-04

Patient: 39 year old female, weighing 55.3 kg (121.7 pounds)

Adverse reactions / side effects: Abdominal Pain, Nausea, Chills, Pyrexia, Hyperhidrosis, Hepatomegaly, Hepatotoxicity, Liver Function Test Abnormal, Liver Tenderness, Sinusitis, Decreased Appetite

Adverse event resulted in: hospitalization

Suspect drug(s):
Avelox
    Dosage: oral
    Administration route: Oral
    Start date: 2007-04-03

Gonal-F
    Dosage: 1 in 1 days, subcutaneous
    Indication: Infertility
    Start date: 2007-03-05
    End date: 2007-03-16

Other drugs received by patient: Crinone



Adverse event in 84 year old male receiving Avelox (Moxifloxacin)

Reported by a physician from United States on 2007-04-20

Patient: 84 year old male

Adverse reactions / side effects: Nephritis Interstitial, Face Oedema, Blood Urine Present, Blood Creatine Phosphokinase Increased, Nausea, Dizziness, Rash, Renal Failure Acute

Adverse event resulted in: hospitalization

Suspect drug(s):
Avelox (Moxifloxacin)



Adverse event in 49 year old female receiving Avelox (Moxifloxacin)

Reported by a physician from United States on 2007-04-02

Patient: 49 year old female, weighing 57.0 kg (125.4 pounds)

Adverse reactions / side effects: Pruritus, Angina Unstable, Anaphylactic Reaction, Headache, Chest Pain, Myocardial Infarction, Dyspnoea, Blood Urine Present, Rash Generalised, Nausea, Urinary Tract Infection, Hypoaesthesia, Respiratory Rate Decreased, Burning Sensation, Heart Rate Decreased, Cardiac Failure, Respiratory Arrest, Blood Pressure Decreased

Adverse event resulted in: hospitalization

Suspect drug(s):
Avelox (Moxifloxacin)

Other drugs received by patient: Vitamin E; Aspirin



Adverse event in 50 year old male receiving Avelox (Moxifloxacin)

Reported by a health professional (non-physician/pharmacist) from United States on 2007-03-30

Patient: 50 year old male

Adverse reactions / side effects: Pancreatitis Acute, Abdominal Pain, Nausea, Eating Disorder, Abdominal Pain Upper, Fatigue, Diarrhoea, Abdominal Distension, Asthenia, Muscle Spasms

Adverse event resulted in: hospitalization

Suspect drug(s):
Avelox (Moxifloxacin)

Other drugs received by patient: Prandin; Glucovance; Metformin; Avandia



Adverse event in 43 year old male receiving Avelox (Moxifloxacin)

Reported by a consumer/non-health professional from United States on 2007-03-23

Patient: 43 year old male, weighing 120.2 kg (264.4 pounds)

Adverse reactions / side effects: Blood Pressure Increased, Back Pain, Dyspnoea, Nausea, Sensation of Heaviness, Chills, Fear, Paraesthesia, Insomnia, Heart Rate Increased

Adverse event resulted in: hospitalization

Suspect drug(s):
Avelox (Moxifloxacin)



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



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