|
Index of reports
> Cases resulting in other serious reactions (103)
> Cases with Haemorrhage (12)
Below is the selection of adverse event reports related to Lovenox (Enoxaparin) that includes cases resulting in other serious reactions where reactions include haemorrhage.
Adverse event in female receiving Lovenox (Enoxaparin)
Reported by a consumer/non-health professional from United States on 2007-10-05
Patient: female, weighing 81.8 kg (180.0 pounds)
Adverse reactions / side effects: Contusion, Drug Ineffective, Haemorrhage, Skin Exfoliation, Headache, Hemiparesis, Appendicitis Perforated, Dermatitis, Skin Discolouration, Transient Ischaemic Attack, Umbilical Hernia, Epistaxis, Injection Site Nodule, Laryngeal Disorder, Cellulitis, Paraesthesia Oral, Muscular Weakness, Atrial Fibrillation, Hypoaesthesia, Peritonitis, Tremor, Sepsis
Adverse event resulted in: hospitalization
Suspect drug(s):
Lovenox
Indication: Atrial Fibrillation
Start date: 2004-01-01
End date: 2007-01-10
Lovenox
Lovenox
Start date: 2007-01-23
Lovenox
Start date: 2004-01-01
End date: 2007-01-10
Lovenox
Lovenox
Start date: 2007-01-23
Other drugs received by patient: Benicar; Toprol-XL; Rythmol / 00546302 /; Rythmol / 00546302 /; Lipitor; Nexium
Adverse event in male receiving Lovenox (Enoxaparin)
Reported by a health professional (non-physician/pharmacist) from United States on 2007-07-09
Patient: male
Adverse reactions / side effects: Injection Site Haemorrhage, Haemorrhage, Alopecia, Injection Site Bruising, Deep Vein Thrombosis
Adverse event resulted in: hospitalization
Suspect drug(s):
Aspirin
Administration route: Oral
Indication: Deep Vein Thrombosis
Start date: 2005-08-01
Coumadin
Dosage: unk
Administration route: Oral
Indication: Deep Vein Thrombosis
Start date: 2005-08-01
End date: 2007-02-01
Lovenox
Indication: Deep Vein Thrombosis
Start date: 2007-02-01
End date: 2007-05-01
Lovenox
Start date: 2007-05-01
Plavix
Administration route: Oral
Indication: Stent Placement
Start date: 2006-01-01
Other drugs received by patient: Risperdal; Toprol-XL; Topamax; Singulair; Advair Diskus 100 / 50; Zetia; Lipitor
Adverse event in female receiving Lovenox (Enoxaparin)
Reported by a consumer/non-health professional from United States on 2007-06-22
Patient: female
Adverse reactions / side effects: Drug Exposure During Pregnancy, Haemorrhage, Platelet Count Decreased, Abortion Spontaneous
Suspect drug(s):
Lovenox (Enoxaparin)
Adverse event in female receiving Lovenox (Enoxaparin)
Reported by a physician from United States on 2007-04-02
Patient: female, weighing 2.8 kg (6.1 pounds)
Adverse reactions / side effects: Retinal Detachment, Prothrombin Time Prolonged, Activated Partial Thromboplastin Time Prolonged, Nystagmus, Foetal Heart Rate Deceleration, Hypoxia, Hypocalcaemia, Blood Creatinine Increased, Blood Gases Abnormal, Aphakia, Disabled Relative, Coombs Test Positive, Blood Fibrinogen Increased, Convulsion, Irritability, White Blood Cell Count Abnormal, Subarachnoid Haemorrhage, Cerebral Infarction, Nervous System Disorder, Haemoglobin Increased, Stridor, Intraventricular Haemorrhage, Haemorrhage, Anaphylactic Shock, Hemiparesis, Fall, Eye Haemorrhage, Hypoacusis, Meconium Stain, Hearing Impaired, Thrombocytopenia, Lethargy, Mental Retardation Severity Unspecified, Neuropathy, Cerebral Palsy, Apgar Score LOW, Blood Urea Increased, Blood Potassium Increased, Iridocele, Subdural Haemorrhage, Haematocrit Increased, Unequal Limb Length, Traumatic Brain Injury, Visual Disturbance, Sepsis
Adverse event resulted in: life threatening event, hospitalization, disablity
Suspect drug(s):
Lovenox (Enoxaparin)
Adverse event in female receiving Lovenox (Enoxaparin)
Reported by a physician from United States on 2007-03-26
Patient: female, weighing 2.8 kg (6.1 pounds)
Adverse reactions / side effects: Retinal Detachment, Prothrombin Time Prolonged, Activated Partial Thromboplastin Time Prolonged, Nystagmus, Foetal Heart Rate Deceleration, Hypocalcaemia, Hypoxia, Blood Creatinine Increased, Aphakia, Blood Gases Abnormal, Disabled Relative, Coombs Test Positive, Blood Fibrinogen Increased, Convulsion, Irritability, White Blood Cell Count Abnormal, Subarachnoid Haemorrhage, Cerebral Infarction, Nervous System Disorder, Haemoglobin Increased, Stridor, Haemorrhage, Intraventricular Haemorrhage, Anaphylactic Shock, Hemiparesis, Fall, Eye Haemorrhage, Hypoacusis, Meconium Stain, Thrombocytopenia, Lethargy, Mental Retardation Severity Unspecified, Cerebral Palsy, Neuropathy, Blood Urea Increased, Blood Potassium Increased, Iridocele, Subdural Haemorrhage, Haematocrit Increased, Unequal Limb Length, Traumatic Brain Injury, Visual Disturbance, Sepsis
Adverse event resulted in: life threatening event, hospitalization, disablity
Suspect drug(s):
Lovenox (Enoxaparin)
Adverse event in female receiving Lovenox (Enoxaparin)
Reported by a physician from United States on 2007-03-15
Patient: female, weighing 2.8 kg (6.1 pounds)
Adverse reactions / side effects: Retinal Detachment, Prothrombin Time Prolonged, Activated Partial Thromboplastin Time Prolonged, Nystagmus, Foetal Heart Rate Deceleration, Hypocalcaemia, Hypoxia, Blood Creatinine Increased, Aphakia, Blood Gases Abnormal, Disabled Relative, Coombs Test Positive, Blood Fibrinogen Increased, Convulsion, Irritability, White Blood Cell Count Abnormal, Subarachnoid Haemorrhage, Cerebral Infarction, Nervous System Disorder, Haemoglobin Increased, Stridor, Haemorrhage, Intraventricular Haemorrhage, Anaphylactic Shock, Hemiparesis, Fall, Eye Haemorrhage, Hypoacusis, Meconium Stain, Thrombocytopenia, Lethargy, Mental Retardation Severity Unspecified, Cerebral Palsy, Neuropathy, Blood Urea Increased, Blood Potassium Increased, Iridocele, Subdural Haemorrhage, Haematocrit Increased, Unequal Limb Length, Traumatic Brain Injury, Visual Disturbance, Sepsis
Adverse event resulted in: life threatening event, hospitalization, disablity
Suspect drug(s):
Lovenox (Enoxaparin)
Adverse event in female receiving Lovenox (Enoxaparin)
Reported by a physician from United States on 2007-03-07
Patient: female, weighing 2.8 kg (6.1 pounds)
Adverse reactions / side effects: Retinal Detachment, Prothrombin Time Prolonged, Activated Partial Thromboplastin Time Prolonged, Nystagmus, Foetal Heart Rate Deceleration, Hypocalcaemia, Hypoxia, Blood Creatinine Increased, Aphakia, Blood Gases Abnormal, Disabled Relative, Coombs Test Positive, Blood Fibrinogen Increased, Convulsion, Irritability, White Blood Cell Count Abnormal, Subarachnoid Haemorrhage, Cerebral Infarction, Nervous System Disorder, Haemoglobin Increased, Stridor, Haemorrhage, Intraventricular Haemorrhage, Anaphylactic Shock, Hemiparesis, Fall, Eye Haemorrhage, Hypoacusis, Meconium Stain, Thrombocytopenia, Lethargy, Mental Retardation Severity Unspecified, Cerebral Palsy, Neuropathy, Blood Urea Increased, Blood Potassium Increased, Iridocele, Subdural Haemorrhage, Haematocrit Increased, Unequal Limb Length, Traumatic Brain Injury, Visual Disturbance, Sepsis
Adverse event resulted in: life threatening event, hospitalization, disablity
Suspect drug(s):
Lovenox (Enoxaparin)
Adverse event in female receiving Lovenox (Enoxaparin)
Reported by a physician from United States on 2007-03-07
Patient: female, weighing 74.5 kg (164.0 pounds)
Adverse reactions / side effects: Chorioamnionitis, Contusion, Haemorrhage, Placental Infarction, Blood Albumin Decreased, Platelet Count Increased, Injection Site Irritation, Blood Magnesium Decreased, Placental Insufficiency, Hospitalisation, Fatigue, Haematocrit Decreased, Liver Function Test Abnormal, Skeletal Injury, White Blood Cell Count Increased, RIB Fracture, Lethargy, Blood Alkaline Phosphatase Increased, Phlebitis, Gingival Bleeding, Pleurisy, Alanine Aminotransferase Increased, Musculoskeletal Chest Pain, Haemoglobin Decreased, RED Blood Cell Morphology Abnormal, Umbilical Cord Abnormality, Arthralgia, Aspartate Aminotransferase Increased, Vasculitis
Adverse event resulted in: hospitalization
Suspect drug(s):
Lovenox
Indication: Deep Vein Thrombosis
Start date: 2002-07-31
End date: 2002-08-01
Lovenox
Start date: 2003-02-19
End date: 2003-02-21
Lovenox
Dosage: dose: unk
Start date: 2003-02-24
Lovenox
Start date: 2003-02-01
End date: 2003-07-24
Lovenox
End date: 2003-07-01
Lovenox
Start date: 2003-07-28
End date: 2003-07-28
Lovenox
Start date: 2006-07-28
Other drugs received by patient: Nubain / 00534802 /; Pitocin; Percocet / 00867901 /; Xanax; Demerol; Dilaudid / 00080902 /; Ativan; Phenergan HCL; Tylenol; Vitamins; Coumadin; Acidophilus; Ambien; Zofran
Adverse event in female receiving Lovenox (Enoxaparin)
Reported by a physician from United States on 2007-03-05
Patient: female, weighing 74.5 kg (164.0 pounds)
Adverse reactions / side effects: Chorioamnionitis, Contusion, Haemorrhage, Placental Infarction, Blood Albumin Decreased, Platelet Count Increased, Injection Site Irritation, Blood Magnesium Decreased, Placental Insufficiency, Hospitalisation, Fatigue, Haematocrit Decreased, Liver Function Test Abnormal, Skeletal Injury, White Blood Cell Count Increased, RIB Fracture, Lethargy, Blood Alkaline Phosphatase Increased, Phlebitis, Gingival Bleeding, Pleurisy, Alanine Aminotransferase Increased, Musculoskeletal Chest Pain, Haemoglobin Decreased, RED Blood Cell Morphology Abnormal, Umbilical Cord Abnormality, Arthralgia, Aspartate Aminotransferase Increased, Vasculitis
Adverse event resulted in: hospitalization
Suspect drug(s):
Lovenox
Indication: Deep Vein Thrombosis
Start date: 2002-07-31
End date: 2002-08-01
Lovenox
Start date: 2003-02-19
End date: 2003-02-21
Lovenox
Dosage: dose: unk
Start date: 2003-02-24
Lovenox
Start date: 2003-02-01
End date: 2003-07-24
Lovenox
End date: 2003-07-01
Lovenox
Start date: 2003-07-28
End date: 2003-07-28
Lovenox
Start date: 2006-07-28
Other drugs received by patient: Nubain / 00534802 /; Pitocin; Percocet / 00867901 /; Xanax; Demerol; Dilaudid / 00080902 /; Ativan; Phenergan HCL; Tylenol; Vitamins; Coumadin; Acidophilus; Ambien; Zofran
Adverse event in female receiving Lovenox (Enoxaparin)
Reported by a physician from United States on 2007-03-01
Patient: female, weighing 74.5 kg (164.0 pounds)
Adverse reactions / side effects: Contusion, Chorioamnionitis, Haemorrhage, Placental Infarction, Blood Albumin Decreased, Platelet Count Increased, Injection Site Irritation, Blood Magnesium Decreased, Placental Insufficiency, Hospitalisation, Haematocrit Decreased, Fatigue, Liver Function Test Abnormal, Skeletal Injury, White Blood Cell Count Increased, RIB Fracture, Lethargy, Blood Alkaline Phosphatase Increased, Phlebitis, Gingival Bleeding, Pleurisy, Alanine Aminotransferase Increased, Musculoskeletal Chest Pain, Haemoglobin Decreased, RED Blood Cell Morphology Abnormal, Umbilical Cord Abnormality, Arthralgia, Drug Exposure During Pregnancy, Aspartate Aminotransferase Increased, Vasculitis
Adverse event resulted in: hospitalization
Suspect drug(s):
Lovenox
Indication: Deep Vein Thrombosis
Start date: 2002-07-31
End date: 2002-08-01
Lovenox
Start date: 2003-02-19
End date: 2003-02-21
Lovenox
Dosage: dose: unk
Start date: 2003-02-24
Lovenox
Start date: 2003-02-01
End date: 2003-07-24
Lovenox
End date: 2003-07-01
Lovenox
Start date: 2003-07-28
End date: 2003-07-28
Lovenox
Start date: 2006-07-28
Other drugs received by patient: Nubain / 00534802 /; Pitocin; Percocet / 00867901 /; Xanax; Demerol; Dilaudid / 00080902 /; Ativan; Phenergan HCL; Tylenol; Vitamins; Coumadin; Acidophilus; Ambien; Zofran
Adverse event in receiving Lovenox (Enoxaparin)
Reported by a consumer/non-health professional from United States on 2007-02-26
Patient:
Adverse reactions / side effects: Death, Drug Ineffective, Haemorrhage, Platelet Count Decreased, Deep Vein Thrombosis
Adverse event resulted in: death
Suspect drug(s):
Lovenox (Enoxaparin)
Adverse event in female receiving Lovenox (Enoxaparin)
Reported by a physician from United States on 2007-02-15
Patient: female, weighing 2.8 kg (6.1 pounds)
Adverse reactions / side effects: Retinal Detachment, Prothrombin Time Prolonged, Activated Partial Thromboplastin Time Prolonged, Nystagmus, Foetal Heart Rate Deceleration, Hypocalcaemia, Hypoxia, Blood Creatinine Increased, Aphakia, Blood Gases Abnormal, Disabled Relative, Coombs Test Positive, Blood Fibrinogen Increased, Convulsion, Irritability, White Blood Cell Count Abnormal, Subarachnoid Haemorrhage, Cerebral Infarction, Nervous System Disorder, Haemoglobin Increased, Stridor, Haemorrhage, Intraventricular Haemorrhage, Anaphylactic Shock, Hemiparesis, Fall, Eye Haemorrhage, Hypoacusis, Meconium Stain, Thrombocytopenia, Lethargy, Mental Retardation Severity Unspecified, Cerebral Palsy, Neuropathy, Blood Urea Increased, Blood Potassium Increased, Iridocele, Subdural Haemorrhage, Haematocrit Increased, Unequal Limb Length, Traumatic Brain Injury, Visual Disturbance, Sepsis
Adverse event resulted in: life threatening event, hospitalization, disablity
Suspect drug(s):
Lovenox (Enoxaparin)
|
