|
This is an index of adverse event reports related to Ludiomil (Maprotiline). Click on the relevant link below to view a selection of reports according to the event's seriousness level and/or the nature of the adverse reaction. Or scroll down to view a sample of recent reports further on this page.
Our database includes reports from Jan 2007 to Dec 2007. The information is not vetted and should not be cosidered as verified clinical evidence.
All cases (48)
Cases resulting in a serious event (48)
Cases resulting in death (2)
Cases resulting in life threatening events (2)
Cases resulting in hospitalization (25)
Cases resulting in disability (2)
Cases resulting in other serious reactions (23)
Below is a sample of adverse event reports reports related to Ludiomil (Maprotiline). For a complete list and/or a specific selection of reports, please use the links in the index above.
Adverse event in 23 year old male receiving Ludiomil (Maprotiline)
Reported by a health professional (non-physician/pharmacist) from Japan on 2007-10-30
Patient: 23 year old male, weighing 74.0 kg (162.8 pounds)
Adverse reactions / side effects: Rhabdomyolysis, Psychomotor Hyperactivity, Body Temperature Increased, Drug Screen Positive, Hyperpyrexia, Convulsion, Drug Toxicity, Cardio-Respiratory Arrest, Antidepressant Drug Level Above Therapeutic, Pulmonary Congestion, Pulmonary Oedema, Multiple Drug Overdose
Adverse event resulted in: death, life threatening event
Suspect drug(s):
Amoxapine
Administration route: Oral
Anafranil
Administration route: Oral
Ludiomil
Administration route: Oral
Indication: Depression
Toledomin
Tryptanol
Administration route: Oral
Adverse event in 23 year old male receiving Ludiomil (Maprotiline)
Reported by a health professional (non-physician/pharmacist) from Japan on 2007-10-22
Patient: 23 year old male, weighing 74.0 kg (162.8 pounds)
Adverse reactions / side effects: Rhabdomyolysis, Psychomotor Hyperactivity, Body Temperature Increased, Drug Screen Positive, Hyperpyrexia, Convulsion, Drug Toxicity, Cardio-Respiratory Arrest, Antidepressant Drug Level Above Therapeutic, Pulmonary Congestion, Pulmonary Oedema, Multiple Drug Overdose
Adverse event resulted in: death, life threatening event
Suspect drug(s):
Amoxapine
Administration route: Oral
Anafranil
Administration route: Oral
Ludiomil
Administration route: Oral
Indication: Depression
Toledomin
Tryptanol / AUS /
Administration route: Oral
Adverse event in 43 year old male receiving Ludiomil (Maprotiline)
Reported by a physician from Japan on 2007-10-18
Patient: 43 year old male, weighing 70.0 kg (154.0 pounds)
Adverse reactions / side effects: Rash Generalised, Pyrexia, Drug Rash With Eosinophilia and Systemic Symptoms
Adverse event resulted in: hospitalization
Suspect drug(s):
Diovan
Dosage: 20 mg/day
Administration route: Oral
Start date: 2007-07-22
End date: 2007-08-27
Lipitor
Dosage: 10 mg/day
Administration route: Oral
Start date: 2007-08-26
Ludiomil
Dosage: 10 mg/day
Administration route: Oral
Start date: 2007-08-15
End date: 2007-08-27
Melbin
Dosage: 500 mg/day
Administration route: Oral
Start date: 2007-08-10
End date: 2007-08-27
Mexitil
Dosage: 300 mg/day
Administration route: Oral
Indication: Nerve Injury
Start date: 2007-07-20
End date: 2007-08-27
PL Gran.
Dosage: 3 mg/day
Administration route: Oral
Start date: 2007-08-22
End date: 2007-08-24
PL Gran.
Dosage: 3 g/day
Administration route: Oral
Start date: 2007-08-28
End date: 2007-08-29
Tegretol
Dosage: 200 mg/day
Administration route: Oral
Indication: Nerve Injury
Start date: 2007-08-07
End date: 2007-08-27
Adverse event in 43 year old male receiving Ludiomil (Maprotiline)
Reported by a physician from Japan on 2007-10-18
Patient: 43 year old male, weighing 70.0 kg (154.0 pounds)
Adverse reactions / side effects: Rash Generalised, Pyrexia, Drug Rash With Eosinophilia and Systemic Symptoms
Adverse event resulted in: hospitalization
Suspect drug(s):
Diovan
Dosage: 20 mg/day
Administration route: Oral
Start date: 2007-07-22
End date: 2007-08-27
Lipitor
Dosage: 10 mg/day
Administration route: Oral
Start date: 2007-08-26
Ludiomil
Dosage: 10 mg/day
Administration route: Oral
Start date: 2007-08-15
End date: 2007-08-27
Melbin
Dosage: 500 mg/day
Administration route: Oral
Start date: 2007-08-10
End date: 2007-08-27
Mexitil
Dosage: 300 mg/day
Administration route: Oral
Indication: Nerve Injury
Start date: 2007-07-20
End date: 2007-08-27
PL Gran.
Dosage: 3 mg/day
Administration route: Oral
Start date: 2007-08-22
End date: 2007-08-24
PL Gran.
Dosage: 3 g/day
Administration route: Oral
Start date: 2007-08-28
End date: 2007-08-29
Tegretol
Dosage: 200 mg/day
Administration route: Oral
Indication: Nerve Injury
Start date: 2007-08-07
End date: 2007-08-27
Adverse event in male receiving Ludiomil (Maprotiline)
Reported by a health professional (non-physician/pharmacist) from Japan on 2007-10-04
Patient: male, weighing 3.8 kg (8.4 pounds)
Adverse reactions / side effects: Blood Creatine Phosphokinase Increased, Rhabdomyolysis, Myoglobin Urine Present, Hypercreatininaemia, Congenital Central Nervous System Anomaly, Joint Contracture, Muscular Dystrophy, Somnolence, Drug Withdrawal Syndrome Neonatal, Myoglobin Blood Increased, Blood Urine Present, Decreased Activity, Poor Sucking Reflex, Drug Exposure During Pregnancy, Hypotonia, Hyporeflexia, Exercise Lack of, Feeding Disorder, Lissencephaly
Adverse event resulted in: hospitalization
Suspect drug(s):
Alprazolam
Depas
Ludiomil
Adverse event in male receiving Ludiomil (Maprotiline)
Reported by a individual with unspecified qualification from Japan on 2007-10-01
Patient: male, weighing 3.8 kg (8.4 pounds)
Adverse reactions / side effects: Weight Decreased, Rhabdomyolysis, Decreased Activity, Muscular Dystrophy, Drug Withdrawal Syndrome, Somnolence, Stress, Drug Exposure During Pregnancy, Congenital Anomaly, Feeding Disorder
Adverse event resulted in: hospitalization
Suspect drug(s):
Alprazolam
Depas
Ludiomil
Adverse event in 53 year old female receiving Ludiomil (Maprotiline)
Reported by a individual with unspecified qualification from Japan on 2007-07-31
Patient: 53 year old female
Adverse reactions / side effects: Blood Creatine Phosphokinase Increased, Skin Graft, Blood Lactate Dehydrogenase Increased, Alanine Aminotransferase Increased, Coma, Loss of Consciousness, Overdose, Skin Ulcer, Aspartate Aminotransferase Increased, Suicide Attempt, Skin Necrosis, Wound Debridement, Blister
Adverse event resulted in: hospitalization
Suspect drug(s):
Depas
Dosage: unk, unk
Administration route: Oral
Indication: Suicide Attempt
Start date: 2000-10-24
End date: 2000-10-24
Halcion
Dosage: unk, unk
Administration route: Oral
Indication: Suicide Attempt
Start date: 2000-10-24
End date: 2000-10-24
Ludiomil
Dosage: unk, unk
Administration route: Oral
Indication: Suicide Attempt
Start date: 2000-10-24
End date: 2000-10-24
Adverse event in 44 year old male receiving Ludiomil (Maprotiline)
Reported by a pharmacist from Japan on 2007-07-27
Patient: 44 year old male
Adverse reactions / side effects: Intentional Overdose, Suicide Attempt, Coma
Adverse event resulted in: hospitalization
Suspect drug(s):
Lexotan
Dosage: 48 df of 2 mg, once/single
Administration route: Oral
Indication: Incorrect Dose Administered
Start date: 2006-12-01
Ludiomil
Dosage: 30 df of 25 mg, once/single
Administration route: Oral
Indication: Incorrect Dose Administered
Start date: 2006-12-01
Tegretol
Dosage: 6 df, once/single
Administration route: Oral
Indication: Incorrect Dose Administered
Start date: 2006-12-01
Other drugs received by patient: Benzodiazepines
Adverse event in 70 year old female receiving Ludiomil (Maprotiline)
Reported by a physician from Japan on 2007-07-23
Patient: 70 year old female
Adverse reactions / side effects: Interstitial Lung Disease, Eosinophilic Pneumonia
Adverse event resulted in: hospitalization
Suspect drug(s):
Ludiomil (Maprotiline)
Other drugs received by patient: Drug Therapy NOS
Adverse event in 53 year old female receiving Ludiomil (Maprotiline)
Reported by a individual with unspecified qualification from Japan on 2007-07-23
Patient: 53 year old female
Adverse reactions / side effects: Overdose, Skin Ulcer, Coma, Blister
Adverse event resulted in: hospitalization
Suspect drug(s):
Depas
Administration route: Oral
Halcion
Administration route: Oral
Indication: Insomnia
Ludiomil
Administration route: Oral
Adverse event in 60 year old male receiving Ludiomil (Maprotiline)
Reported by a consumer/non-health professional from Brazil on 2007-07-20
Patient: 60 year old male, weighing 50.0 kg (110.0 pounds)
Adverse reactions / side effects: Tinnitus, Dysacusis, Dizziness, Hearing Impaired, Depression, Ear Congestion, Somnolence
Suspect drug(s):
Ludiomil
Dosage: one 25 mg tablet every mon, wed, fri
Administration route: Oral
Indication: Depression
Start date: 2002-01-01
Olcadil
Dosage: 2 mg, tid
Administration route: Oral
Indication: Depression
Start date: 1997-09-25
End date: 2002-01-01
Olcadil
Dosage: half a 1 mg tablet at night
Administration route: Oral
Start date: 2002-01-01
End date: 2007-06-01
Olcadil
Dosage: 1/2 x 1 mg in afternoon and at night
Administration route: Oral
Start date: 2007-06-01
Adverse event in 53 year old female receiving Ludiomil (Maprotiline)
Reported by a individual with unspecified qualification from Japan on 2007-07-18
Patient: 53 year old female
Adverse reactions / side effects: Overdose, Skin Ulcer, Suicide Attempt, Coma, Blister
Adverse event resulted in: hospitalization
Suspect drug(s):
Depas
Administration route: Oral
Indication: Suicide Attempt
Halcion
Administration route: Oral
Indication: Suicide Attempt
Ludiomil
Administration route: Oral
Indication: Suicide Attempt
Adverse event in 28 year old female receiving Ludiomil (Maprotiline)
Reported by a health professional (non-physician/pharmacist) from Switzerland on 2007-07-05
Patient: 28 year old female
Adverse reactions / side effects: Nephrolithiasis, Urinary Tract Infection, Dysuria, Pollakiuria, Renal Pain, Renal Cyst, Urinary Retention
Adverse event resulted in: hospitalization
Suspect drug(s):
Ludiomil (Maprotiline)
Adverse event in 81 year old female receiving Ludiomil (Maprotiline)
Reported by a pharmacist from Japan on 2007-06-28
Patient: 81 year old female
Adverse reactions / side effects: Surgery, Femur Fracture
Suspect drug(s):
Ludiomil (Maprotiline)
Adverse event in 70 year old female receiving Ludiomil (Maprotiline)
Reported by a physician from Japan on 2007-06-20
Patient: 70 year old female
Adverse reactions / side effects: Hyponatraemia
Adverse event resulted in: disablity
Suspect drug(s):
Ludiomil (Maprotiline)
Adverse event in 81 year old female receiving Ludiomil (Maprotiline)
Reported by a pharmacist from Japan on 2007-06-18
Patient: 81 year old female
Adverse reactions / side effects: Surgery, Femur Fracture, Gait Disturbance
Suspect drug(s):
Ludiomil (Maprotiline)
Adverse event in 76 year old male receiving Ludiomil (Maprotiline)
Reported by a health professional (non-physician/pharmacist) from Austria on 2007-06-15
Patient: 76 year old male
Adverse reactions / side effects: Anxiety, Nausea, Unresponsive TO Stimuli, Hyperreflexia, Serotonin Syndrome, Delirium, Hyperhidrosis, Tremor
Suspect drug(s):
Ludiomil
Indication: Depression
Mirtazapine
Quilonorm
Seroxat ^novo Nordisk^
Tramadol HCL
Adverse event in male receiving Ludiomil (Maprotiline)
Reported by a individual with unspecified qualification from Japan on 2007-05-31
Patient: male, weighing 3.8 kg (8.4 pounds)
Adverse reactions / side effects: Blood Creatine Phosphokinase Increased, Rhabdomyolysis, Congenital Central Nervous System Anomaly, Hypercreatininaemia, Joint Contracture, Muscular Dystrophy, Drug Withdrawal Syndrome Neonatal, Somnolence, Myoglobin Blood Increased, Blood Urine Present, Decreased Activity, Poor Sucking Reflex, Drug Exposure During Pregnancy, Hypotonia, Exercise Lack of, Hyporeflexia, Feeding Disorder, Lissencephaly
Adverse event resulted in: hospitalization
Suspect drug(s):
Depas
Ludiomil
Other drugs received by patient: Solanax
Adverse event in 70 year old female receiving Ludiomil (Maprotiline)
Reported by a physician from Japan on 2007-05-31
Patient: 70 year old female
Adverse reactions / side effects: Hyponatraemia
Adverse event resulted in: disablity
Suspect drug(s):
Ludiomil (Maprotiline)
Adverse event in male receiving Ludiomil (Maprotiline)
Reported by a individual with unspecified qualification from Japan on 2007-05-31
Patient: male, weighing 3.8 kg (8.4 pounds)
Adverse reactions / side effects: Blood Creatine Phosphokinase Increased, Rhabdomyolysis, Blood Urine Present, Hypercreatininaemia, Congenital Central Nervous System Anomaly, Joint Contracture, Decreased Activity, Muscular Dystrophy, Somnolence, Drug Withdrawal Syndrome Neonatal, Hypotonia, Myoglobin Blood Increased, Hyporeflexia, Feeding Disorder, Exercise Lack of, Lissencephaly
Adverse event resulted in: hospitalization
Suspect drug(s):
Alprazolam
Etizolam
Ludiomil
Adverse event in 85 year old female receiving Ludiomil (Maprotiline)
Reported by a pharmacist from Japan on 2007-04-13
Patient: 85 year old female
Adverse reactions / side effects: Vomiting, Gastroenteritis
Suspect drug(s):
Ludiomil
Dosage: 10 mg/d
Administration route: Oral
Indication: Depression
Paxil
Dosage: 20 mg/d
Administration route: Oral
Indication: Depression
Other drugs received by patient: Warfarin Sodium; Lanirapid
Adverse event in 50 year old male receiving Ludiomil (Maprotiline)
Reported by a pharmacist from Japan on 2007-04-11
Patient: 50 year old male, weighing 65.0 kg (143.0 pounds)
Adverse reactions / side effects: Blood Creatine Phosphokinase Increased, Hepatic Function Abnormal, Intentional Overdose, Alanine Aminotransferase Increased, Drug Toxicity, Aspartate Aminotransferase Increased, Depressed Level of Consciousness, Suicide Attempt, Muscle Disorder
Adverse event resulted in: hospitalization
Suspect drug(s):
Lexotan
Dosage: 5 mg/day
Administration route: Oral
Indication: Depression
Start date: 2005-12-17
End date: 2007-02-26
Lexotan
Dosage: 140 mg, once/single
Administration route: Oral
Start date: 2007-02-27
End date: 2007-02-27
Ludiomil
Dosage: 25 mg, qd
Administration route: Oral
Indication: Depression
Start date: 2005-12-17
End date: 2006-11-24
Ludiomil
Dosage: 50 mg, qd
Administration route: Oral
Start date: 2006-11-25
End date: 2007-02-26
Ludiomil
Dosage: 2500 mg, once/single
Administration route: Oral
Start date: 2007-02-27
End date: 2007-02-27
Nitrazepam
Dosage: 10 mg/day
Administration route: Oral
Indication: Insomnia
Start date: 2005-12-17
End date: 2007-02-26
Nitrazepam
Dosage: 580 mg, once/single
Administration route: Oral
Start date: 2007-02-27
End date: 2007-02-27
Rohypnol
Dosage: 2 mg/day
Administration route: Oral
Indication: Insomnia
Start date: 2005-12-17
End date: 2007-02-26
Rohypnol
Dosage: 20 mg, once/single
Administration route: Oral
Start date: 2007-02-27
End date: 2007-02-27
Adverse event in male receiving Ludiomil (Maprotiline)
Reported by a individual with unspecified qualification from Japan on 2007-04-11
Patient: male, weighing 3.8 kg (8.4 pounds)
Adverse reactions / side effects: Blood Creatine Phosphokinase Increased, Rhabdomyolysis, Blood Urine Present, Hypercreatininaemia, Congenital Central Nervous System Anomaly, Joint Contracture, Decreased Activity, Muscular Dystrophy, Somnolence, Drug Withdrawal Syndrome Neonatal, Hypotonia, Myoglobin Blood Increased, Hyporeflexia, Feeding Disorder, Exercise Lack of, Lissencephaly
Adverse event resulted in: hospitalization
Suspect drug(s):
Alprazolam
Etizolam
Ludiomil
Adverse event in 77 year old female receiving Ludiomil (Maprotiline)
Reported by a individual with unspecified qualification from Japan on 2007-04-06
Patient: 77 year old female, weighing 51.0 kg (112.2 pounds)
Adverse reactions / side effects: Blood Lactate Dehydrogenase Increased, Chest X-RAY Abnormal, Bronchoalveolar Lavage Abnormal, Fatigue, Palpitations, C-Reactive Protein Increased, Interstitial Lung Disease, Cell Marker Increased, Lung Infiltration, Oxygen Saturation Decreased, White Blood Cell Count Increased
Adverse event resulted in: hospitalization
Suspect drug(s):
Ludiomil
Dosage: 75 mg/d
Administration route: Oral
Indication: Depression
Start date: 2006-08-28
End date: 2006-11-07
Tsumura Byakkokaninjinto
Dosage: 9 g/d
Administration route: Oral
Indication: Thirst
Start date: 2006-09-21
End date: 2006-11-07
Other drugs received by patient: Amoban; Tecipul
Adverse event in male receiving Ludiomil (Maprotiline)
Reported by a individual with unspecified qualification from Japan on 2007-04-06
Patient: male, weighing 3.8 kg (8.4 pounds)
Adverse reactions / side effects: Weight Decreased, Rhabdomyolysis, Decreased Activity, Muscular Dystrophy, Drug Withdrawal Syndrome, Somnolence, Stress, Drug Exposure During Pregnancy, Congenital Anomaly, Feeding Disorder
Adverse event resulted in: hospitalization
Suspect drug(s):
Depas
Ludiomil
Solanax
|
