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Index of reports
> Life Threatening Events (65)
Below is the selection of side effect reports (a.k.a. adverse event reports) related to Neoral (Cyclosporine) life threatening events. The selected reports were submitted to the FDA during the sample period of about a year. Reports 1 - 30 of 65 Next >>
Possible Neoral side effects in female
Reported by a physician from United States on 2012-08-10
Patient: female
Reactions: Sepsis, Myocardial Infarction, Feeling Abnormal
Adverse event resulted in: life threatening event, hospitalization
Drug(s) suspected as cause:
Neoral
Possible Neoral side effects in female
Reported by a health professional (non-physician/pharmacist) from United States on 2012-08-07
Patient: female
Reactions: Pruritus, Rash, Suicidal Ideation
Adverse event resulted in: life threatening event
Drug(s) suspected as cause:
Neoral
Dosage: 100 mg, 2 capsules am, 1 capsule pm
Administration route: Oral
Start date: 2010-10-07
Neoral
Dosage: 2 df, unk
Possible Neoral side effects in 58 year old female
Reported by a physician from France on 2012-07-27
Patient: 58 year old female
Reactions: Central Nervous System Lymphoma
Adverse event resulted in: life threatening event
Drug(s) suspected as cause:
Neoral
Administration route: Oral
Indication: Product Used FOR Unknown Indication
Start date: 2002-09-01
End date: 2011-12-01
Cellcept
Administration route: Oral
Indication: Product Used FOR Unknown Indication
Start date: 2002-01-01
End date: 2011-12-01
Other drugs received by patient: Dedrogyl; Prednisolone; Potassium Chloride; Nexium
Possible Neoral side effects in female
Reported by a physician from Italy on 2012-07-26
Patient: female, weighing 46.0 kg (101.2 pounds)
Reactions: Encephalitis, Coma, Renal Graft Loss
Adverse event resulted in: life threatening event, hospitalization
Drug(s) suspected as cause:
Medrol
Dosage: 4 mg, unk
Administration route: Oral
Indication: Renal Transplant
Start date: 2012-06-13
Neoral
Dosage: 0.75 mg, unk
Administration route: Oral
Indication: Renal Transplant
Start date: 2012-06-13
Certican
Dosage: 1.25 mg, unk
Administration route: Oral
Indication: Renal Transplant
Start date: 2012-06-15
End date: 2012-06-23
Other drugs received by patient: Bactrim; Atenolol; Zovirax; Pantoprazole Sodium
Possible Neoral side effects in female
Reported by a health professional (non-physician/pharmacist) from Argentina on 2012-07-26
Patient: female, weighing 58.0 kg (127.6 pounds)
Reactions: Renal Impairment, Bacteraemia, Ischaemic Stroke, Urinary Tract Infection, Dehydration, Septic Shock, Cardiac Arrest
Adverse event resulted in: death, life threatening event, hospitalization
Drug(s) suspected as cause:
Myfortic
Dosage: 720 mg, bid
Administration route: Oral
Start date: 2011-12-16
End date: 2012-01-24
Neoral
Dosage: unk
Indication: Renal Transplant
Start date: 2012-01-26
End date: 2012-01-28
Prograf
Dosage: 10 mg, unk
Administration route: Oral
Prograf
Dosage: 4 mg, bid
Administration route: Oral
Indication: Renal Transplant
Start date: 2011-12-16
End date: 2012-01-25
Possible Neoral side effects in male
Reported by a health professional (non-physician/pharmacist) from Japan on 2012-07-18
Patient: male
Reactions: Gastrointestinal Haemorrhage, Disseminated Intravascular Coagulation, Enterococcal Infection, Coagulopathy, Cardiac Failure Acute, Pneumonia Cytomegaloviral, Pneumocystis Jiroveci Pneumonia, Anal Fistula, Colonic Fistula, Acute Respiratory Distress Syndrome, Circulatory Collapse, Apnoea, Melaena, Cytomegalovirus Enterocolitis, Metabolic Acidosis, Gastrointestinal Ulcer Haemorrhage, Restlessness, Hyperglycaemia, Anaemia, Duodenal Ulcer, Ulcer, Delirium, Fungal Infection, Insomnia, Systemic Inflammatory Response Syndrome, Septic Shock, Hypoventilation, Oral Administration Complication, Shock Haemorrhagic, Ileal Ulcer, Interstitial Lung Disease, Large Intestinal Ulcer, Ileal Fistula, Small Intestinal Haemorrhage, Acute Respiratory Failure, Dyspnoea, Diarrhoea, Respiratory Failure, Sepsis, Anal Haemorrhage, Purulence, Hypertension
Adverse event resulted in: death, life threatening event
Drug(s) suspected as cause:
Bredinin
Dosage: 100 mg, daily
Administration route: Oral
End date: 2011-03-08
Neoral
Dosage: 100 mg, daily
Administration route: Oral
Start date: 2010-11-18
End date: 2011-03-15
Rituximab
Dosage: unk ukn, unk
Prograf
Dosage: 2 mg, daily
Administration route: Oral
End date: 2011-11-17
Prednisolone
Dosage: 10 mg, unk
End date: 2011-03-22
Prednisolone
Dosage: 10 mg, daily
Administration route: Oral
End date: 2011-03-18
Neoral
Dosage: 50 mg, daily
Administration route: Oral
Indication: Renal Transplant
End date: 2011-03-15
Mycophenolate Mofetil
Indication: Renal Transplant
Other drugs received by patient: Insulin
Possible Neoral side effects in male
Reported by a health professional (non-physician/pharmacist) from Japan on 2012-07-18
Patient: male
Reactions: Gastrointestinal Haemorrhage, Coagulopathy, Disseminated Intravascular Coagulation, Enterococcal Infection, Cardiac Failure Acute, Pneumonia Cytomegaloviral, Anal Fistula, Pneumocystis Jiroveci Pneumonia, Colonic Fistula, Acute Respiratory Distress Syndrome, Circulatory Collapse, Apnoea, Melaena, Cytomegalovirus Enterocolitis, Metabolic Acidosis, Restlessness, Gastrointestinal Ulcer Haemorrhage, Anaemia, Hyperglycaemia, Duodenal Ulcer, Ulcer, Delirium, Fungal Infection, Insomnia, Systemic Inflammatory Response Syndrome, Septic Shock, Hypoventilation, Oral Administration Complication, Shock Haemorrhagic, Ileal Ulcer, Interstitial Lung Disease, Ileal Fistula, Large Intestinal Ulcer, Small Intestinal Haemorrhage, Acute Respiratory Failure, Dyspnoea, Diarrhoea, Respiratory Failure, Sepsis, Purulence, Anal Haemorrhage, Hypertension
Adverse event resulted in: death, life threatening event
Drug(s) suspected as cause:
Rituximab
Dosage: unk ukn, unk
Prednisolone
Dosage: 10 mg, daily
Administration route: Oral
End date: 2011-03-18
Neoral
Dosage: 50 mg, daily
Administration route: Oral
Indication: Renal Transplant
End date: 2011-03-15
Bredinin
Dosage: 100 mg, daily
Administration route: Oral
End date: 2011-03-08
Mycophenolate Mofetil
Indication: Renal Transplant
Prograf
Dosage: 2 mg, daily
Administration route: Oral
End date: 2011-11-17
Neoral
Dosage: 100 mg, daily
Administration route: Oral
Start date: 2010-11-18
End date: 2011-03-15
Prednisolone
Dosage: 10 mg, unk
End date: 2011-03-22
Other drugs received by patient: Insulin
Possible Neoral side effects in male
Reported by a physician from Mexico on 2012-07-13
Patient: male, weighing 48.0 kg (105.6 pounds)
Reactions: Jaundice, Gastrointestinal Haemorrhage, Pneumonia, Complications of Transplanted Kidney, Respiratory Failure, Cytomegalovirus Infection, Acute Respiratory Distress Syndrome, Gastritis
Adverse event resulted in: death, life threatening event, hospitalization
Drug(s) suspected as cause:
Neoral
Dosage: 25 mg, bid
Administration route: Oral
End date: 2012-06-13
Neoral
Dosage: 25 mg, bid
Administration route: Oral
Start date: 2012-06-18
Prednisone
Dosage: 15 mg, qd
Administration route: Oral
Indication: Renal Transplant
Start date: 2012-05-16
End date: 2012-06-13
Neoral
Dosage: 50 mg, bid
Administration route: Oral
Indication: Renal Transplant
Start date: 2012-05-02
Prednisone
Dosage: 15 mg, qd
Administration route: Oral
Other drugs received by patient: Acyclovir; Myfortic; Bactrim; Amlodipine; Myfortic; Nystatin; Metoprolol Tartrate; Losartan Potassium
Possible Neoral side effects in female
Reported by a health professional (non-physician/pharmacist) from Japan on 2012-07-09
Patient: female, weighing 39.0 kg (85.8 pounds)
Reactions: Renal Impairment, Pneumonia, Cardiac Failure, Hypokalaemia
Adverse event resulted in: life threatening event
Drug(s) suspected as cause:
Exjade
Dosage: 1000 mg, daily
Administration route: Oral
Indication: Iron Overload
Start date: 2009-05-27
End date: 2009-07-07
Neoral
Indication: Myelodysplastic Syndrome
Neoral
Dosage: 100 mg, daily
Administration route: Oral
Indication: Iron Overload
Start date: 2009-05-27
End date: 2009-11-24
Exjade
Dosage: 725 mg, daily
Administration route: Oral
Indication: Myelodysplastic Syndrome
Start date: 2009-09-30
End date: 2009-11-24
Other drugs received by patient: Blood Transfusion, Auxiliary Products; Primobolan-Depot INJ; Prednisolone Sodium Succinate INJ; RED Blood Cells, Concentrated; RED Blood Cells, Concentrated
Possible Neoral side effects in male
Reported by a physician from Japan on 2012-07-05
Patient: male
Reactions: Lymphoma
Adverse event resulted in: life threatening event
Drug(s) suspected as cause:
Colchicine
Administration route: Oral
Indication: Product Used FOR Unknown Indication
Remicade
Indication: Behcet's Syndrome
Start date: 2007-08-20
Neoral
Administration route: Oral
Indication: Product Used FOR Unknown Indication
Remicade
Start date: 2012-04-01
Possible Neoral side effects in female
Reported by a health professional (non-physician/pharmacist) from United States on 2012-07-04
Patient: female
Reactions: Stress, Rash Pruritic, Suicidal Ideation
Adverse event resulted in: life threatening event
Drug(s) suspected as cause:
Neoral
Possible Neoral side effects in female
Reported by a physician from Italy on 2012-06-28
Patient: female, weighing 46.0 kg (101.2 pounds)
Reactions: Central Nervous System Infection, Coma
Adverse event resulted in: life threatening event, hospitalization
Drug(s) suspected as cause:
Neoral
Dosage: 0.75 mg, unk
Administration route: Oral
Indication: Renal Transplant
Start date: 2012-06-13
Certican
Dosage: 1.25 mg, unk
Administration route: Oral
Indication: Renal Transplant
Start date: 2012-06-15
End date: 2012-06-23
Medrol
Dosage: 4 mg, unk
Administration route: Oral
Indication: Renal Transplant
Start date: 2012-06-13
Other drugs received by patient: Bactrim; Pantoprazole Sodium; Atenolol; Zovirax
Possible Neoral side effects in female
Reported by a physician from Italy on 2012-06-28
Patient: female
Reactions: Central Nervous System Infection, Coma, Convulsion
Adverse event resulted in: life threatening event, hospitalization
Drug(s) suspected as cause:
Medrol
Dosage: 4 mg, unk
Administration route: Oral
Indication: Renal Transplant
Start date: 2012-06-13
Neoral
Dosage: 75 mg, bid
Administration route: Oral
Indication: Renal Transplant
Start date: 2012-06-13
Other drugs received by patient: Bactrim; Atenolol; Pantoprazole Sodium; Zovirax
Possible Neoral side effects in male
Reported by a physician from Japan on 2012-06-18
Patient: male, weighing 72.0 kg (158.4 pounds)
Reactions: Urine Output Decreased, Pancytopenia, Condition Aggravated, Pyrexia, Ascites, Renal Failure, Renal Impairment, Hepatic Cirrhosis
Adverse event resulted in: life threatening event
Drug(s) suspected as cause:
Neoral
Dosage: 420 mg, qd
Administration route: Oral
Indication: Aplastic Anaemia
Start date: 2012-04-13
End date: 2012-04-19
Neoral
Dosage: 250 mg, qd
Administration route: Oral
Start date: 2012-04-20
End date: 2012-04-20
Neoral
Dosage: 125 mg, unk
Administration route: Oral
Start date: 2012-05-10
End date: 2012-05-10
Neoral
Dosage: 75 mg, unk
Administration route: Oral
Start date: 2012-05-11
End date: 2012-05-13
Neoral
Dosage: 150 mg, unk
Administration route: Oral
Start date: 2012-04-21
End date: 2012-05-09
Other drugs received by patient: Adrenal Hormone Preparations; Omeprazole; Primobolan-Depot INJ; Diflucan; Losartan Potassium; Sodium Chloride; Corticosteroid NOS; Pursennid; Gran; Pyrinazin; Solu-Medrol; Thymoglobulin; Lactec; Lactec; Omeprazole; Valtrex
Possible Neoral side effects in female
Reported by a consumer/non-health professional from Japan on 2012-06-11
Patient: female
Reactions: Protein Urine Present, Blood Urea Increased, Hyperglycaemia, Muscular Weakness, Loss of Consciousness, Weight Increased, Renal Failure, Cardiac Failure, Oedema, Arthritis Bacterial, Gait Disturbance, Necrotising Fasciitis
Adverse event resulted in: life threatening event, hospitalization
Drug(s) suspected as cause:
Neoral
Other drugs received by patient: Adrenocorticotrophic Hormone; Adrenocorticotrophic Hormone; Corticosteroids
Possible Neoral side effects in female
Reported by a consumer/non-health professional from Japan on 2012-06-06
Patient: female
Reactions: Weight Increased, Protein Urine Present, Renal Failure, Cardiac Failure, Oedema, Arthritis Bacterial, Muscular Weakness, Gait Disturbance, Necrotising Fasciitis, Loss of Consciousness
Adverse event resulted in: life threatening event, hospitalization
Drug(s) suspected as cause:
Neoral
Other drugs received by patient: Adrenocorticotrophic Hormone; Adrenocorticotrophic Hormone
Possible Neoral side effects in female
Reported by a consumer/non-health professional from Japan on 2012-06-04
Patient: female
Reactions: Weight Increased, Protein Urine Present, Renal Failure, Cardiac Failure, Oedema, Muscular Weakness, Gait Disturbance, Necrotising Fasciitis, Loss of Consciousness
Adverse event resulted in: life threatening event, hospitalization
Drug(s) suspected as cause:
Neoral
Other drugs received by patient: Adrenocorticotrophic Hormone; Adrenocorticotrophic Hormone
Possible Neoral side effects in 45 year old female
Reported by a health professional (non-physician/pharmacist) from France on 2012-05-23
Patient: 45 year old female, weighing 60.0 kg (132.0 pounds)
Reactions: Confusional State, Dyskinesia, Hypotonia, Altered State of Consciousness
Adverse event resulted in: life threatening event
Drug(s) suspected as cause:
Fludarabine Phosphate
Dosage: 68 mg, unk
Indication: Cord Blood Transplant Therapy
Start date: 2012-01-05
End date: 2012-01-08
Cyclophosphamide
Dosage: 1905 mg, unk
Indication: Cord Blood Transplant Therapy
Start date: 2012-01-05
End date: 2012-01-06
Thymoglobulin
Dosage: 476 mg, unk
Indication: Cord Blood Transplant Therapy
Start date: 2012-01-09
End date: 2012-01-10
Neoral
Dosage: unk
Start date: 2011-10-29
End date: 2012-01-15
Targocid
Dosage: 400 mg, 1x/day
Start date: 2011-12-27
End date: 2012-01-15
Vfend
Dosage: 400 mg, 1x/day
Indication: Candidiasis
Start date: 2011-12-30
End date: 2012-01-15
Cefepime
Dosage: 6 g, 1x/day
Indication: Cord Blood Transplant Therapy
Start date: 2011-12-30
End date: 2012-01-15
Possible Neoral side effects in female
Reported by a health professional (non-physician/pharmacist) from Japan on 2012-05-18
Patient: female, weighing 56.0 kg (123.2 pounds)
Reactions: Abdominal Pain, Body Temperature Increased, Haemorrhage, Disseminated Intravascular Coagulation, Blood Albumin Decreased, Wound Haemorrhage, Postoperative Abscess, Skin Discolouration, C-Reactive Protein Increased, RED Blood Cell Count Decreased, Skin Ulcer, Skin Atrophy, White Blood Cell Count Increased, Blister, Large Intestine Perforation, Blood Lactate Dehydrogenase Increased, Anaemia, Hypotension, Skin Fragility, Protein Total Decreased, Purpura, Nephrotic Syndrome, Haemoglobin Decreased, Impaired Healing, Heart Rate Increased, Sepsis, Platelet Count Decreased, Skin Infection, Necrotising Fasciitis, Escherichia Infection, Shock
Adverse event resulted in: life threatening event, hospitalization
Drug(s) suspected as cause:
Bredinin
Dosage: 150 mg, unk
Administration route: Oral
Indication: Nephrotic Syndrome
Start date: 2009-03-11
End date: 2010-06-02
Neoral
Dosage: 150 mg, unk
Administration route: Oral
Indication: Nephrotic Syndrome
Start date: 2000-05-01
Prednisolone
Dosage: 35 mg, unk
Administration route: Oral
Indication: Nephrotic Syndrome
Start date: 1998-01-01
Other drugs received by patient: Slow-K; Humulin R; Steroids NOS; Locholest; Prednisolone; Alendronate Sodium; Lasix; Humulin N
Possible Neoral side effects in female
Reported by a health professional (non-physician/pharmacist) from France on 2012-05-16
Patient: female
Reactions: Confusional State, Dyskinesia, Hypotonia, Altered State of Consciousness
Adverse event resulted in: life threatening event
Drug(s) suspected as cause:
Neoral
Start date: 2011-10-29
End date: 2012-01-15
Fludarabine Phosphate
Indication: Cord Blood Transplant Therapy
Start date: 2012-01-05
End date: 2012-01-08
Vfend
Start date: 2011-12-30
End date: 2012-01-15
Cyclophosphamide
Indication: Cord Blood Transplant Therapy
Start date: 2012-01-05
End date: 2012-01-06
Thymoglobulin
Indication: Cord Blood Transplant Therapy
Start date: 2012-01-09
End date: 2012-01-10
Cefepime
Indication: Cord Blood Transplant Therapy
Start date: 2011-12-30
End date: 2012-01-15
Targocid
Start date: 2011-12-27
End date: 2012-01-15
Possible Neoral side effects in male
Reported by a health professional (non-physician/pharmacist) from Japan on 2012-05-16
Patient: male, weighing 66.0 kg (145.2 pounds)
Reactions: Multi-Organ Failure, Pneumocystis Jiroveci Pneumonia, Gastroenteritis Norovirus, Renal Disorder, Respiratory Failure, Liver Disorder
Adverse event resulted in: death, life threatening event
Drug(s) suspected as cause:
Neoral
Other drugs received by patient: Venoglobulin; Meropenem; Prednisolone; Vfend; Rabeprazole Sodium; Pacil
Possible Neoral side effects in female
Reported by a health professional (non-physician/pharmacist) from Japan on 2012-05-10
Patient: female, weighing 56.0 kg (123.2 pounds)
Reactions: Abdominal Pain, Body Temperature Increased, Haemorrhage, Disseminated Intravascular Coagulation, Blood Albumin Decreased, Wound Haemorrhage, Postoperative Abscess, RED Blood Cell Count Decreased, C-Reactive Protein Increased, Skin Ulcer, Skin Discolouration, Skin Atrophy, White Blood Cell Count Increased, Blister, Large Intestine Perforation, Hypotension, Anaemia, Blood Lactate Dehydrogenase Increased, Skin Fragility, Purpura, Protein Total Decreased, Nephrotic Syndrome, Haemoglobin Decreased, Impaired Healing, Sepsis, Heart Rate Increased, Platelet Count Decreased, Skin Infection, Necrotising Fasciitis, Escherichia Infection, Shock
Adverse event resulted in: life threatening event, hospitalization
Drug(s) suspected as cause:
Neoral
Dosage: 150 mg, unk
Administration route: Oral
Indication: Nephrotic Syndrome
Start date: 2000-05-01
Prednisolone
Dosage: 35 mg, unk
Administration route: Oral
Indication: Nephrotic Syndrome
Start date: 1998-01-01
Prednisolone
Dosage: 2 mg, unk
Administration route: Oral
Indication: Nephrotic Syndrome
Start date: 1998-01-01
Bredinin
Dosage: 150 mg, unk
Administration route: Oral
Indication: Nephrotic Syndrome
Start date: 2009-03-11
End date: 2010-06-02
Other drugs received by patient: Locholest; Slow-K; Humulin N; Steroids NOS; Lasix; Humulin R; Alendronate Sodium
Possible Neoral side effects in 57 year old female
Reported by a physician from Ireland on 2012-04-24
Patient: 57 year old female
Reactions: Dyslipidaemia, Lymphadenopathy, Mouth Ulceration, Dental Plaque, IGA Nephropathy, Headache, Hepatomegaly, Blood Creatinine Increased, Lethargy, Muscle Spasms, Dyspnoea, Pulmonary Sarcoidosis, Toxicity To Various Agents, Nephrotic Syndrome, Tremor, Anxiety, Antinuclear Antibody Positive, Gingival Pain, Joint Swelling, Lymphoma, Asthenia, Normochromic Normocytic Anaemia, Hypertension
Adverse event resulted in: life threatening event, hospitalization, disablity
Drug(s) suspected as cause:
Toviaz
Dosage: 4 mg, unk
Administration route: Oral
Indication: Hypertonic Bladder
Cyclosporine
Dosage: 125 mg, 2x/day
Neoral
Dosage: unk
Neoral
Dosage: 125mg mane/100mg nocte
Start date: 2011-04-13
Other drugs received by patient: Calcichew-D3; Lansoprazole; Bumetanide; Fosamax; Acetylsalicylic Acid; Ramipril; Ramipril; Amlodipine; Furosemide; Prednisolone; Alendronate Sodium; Lansoprazole; Lercanidipine; Atorvastatin; Prednisolone; Bumetanide
Possible Neoral side effects in 25 year old male
Reported by a consumer/non-health professional from Japan on 2012-04-23
Patient: 25 year old male, weighing 57.0 kg (125.4 pounds)
Reactions: Eyelid Oedema, Pneumonia Viral, Gastrointestinal Haemorrhage, Hepatic Function Abnormal, Graft Versus Host Disease, Disseminated Intravascular Coagulation, Headache, Pyrexia, Oral Herpes, Pneumonia Cytomegaloviral, Generalised Oedema, Pericardial Effusion, Pneumocystis Jiroveci Pneumonia, Interstitial Lung Disease, Liver Function Test Abnormal, Pleural Effusion, Enterocolitis, Bronchopulmonary Aspergillosis, White Blood Cell Count Decreased, Anaemia, Pulmonary Haemorrhage, Renal Impairment, Platelet Count Decreased, Neutrophil Count Decreased
Adverse event resulted in: death, life threatening event, hospitalization
Drug(s) suspected as cause:
Itraconazole
Dosage: capsule;400-200mg/day(06jul-16jul09)inj.
Administration route: Oral
Indication: Prophylaxis
Start date: 2009-06-06
End date: 2009-07-16
Foscavir
Dosage: form:inj1 df= 10 unit nos
Start date: 2009-07-10
End date: 2009-07-16
Bactrim
Dosage: 1df=1tab;800mg/day(02jul-18jul09)inj.
Administration route: Oral
Indication: Antibiotic Prophylaxis
Start date: 2009-04-14
End date: 2009-07-16
Farom
Administration route: Oral
Start date: 2009-04-28
End date: 2009-05-01
Neoral
Dosage: 09jul-16jul09. 125mg/day sandimmun:inj:50mg/dy:09jul-16jul09
Administration route: Oral
Indication: Prophylaxis
Start date: 2009-04-14
End date: 2009-07-08
Sprycel
Administration route: Oral
Indication: Acute Lymphocytic Leukaemia
Start date: 2009-04-16
End date: 2009-07-08
Maxipime
Start date: 2009-04-24
End date: 2009-04-27
Other drugs received by patient: Ceftazidime; Solu-Medrol; Ambisome; Piperacillin and Tazobactam; Pentamidine Isethionate; Ganciclovir; Meropenem; Omegacin; Sandimmune; Prednisolone
Possible Neoral side effects in male
Reported by a physician from France on 2012-04-20
Patient: male, weighing 68.0 kg (149.6 pounds)
Reactions: Bronchial Obstruction, Klebsiella Infection, Thrombocytopenia, Post Procedural Haemorrhage, Escherichia Sepsis, Renal Vessel Disorder, Complications of Transplanted Kidney, Wound Dehiscence, Anaemia, Malnutrition, Anastomotic Haemorrhage, Wound Complication, Renal Impairment, Diarrhoea, Cytomegalovirus Infection, Renal Tubular Necrosis, Pneumonia Escherichia, Asthenia, Leukopenia
Adverse event resulted in: death, life threatening event, hospitalization
Drug(s) suspected as cause:
Neoral
Dosage: 400 mg, qd
Administration route: Oral
Start date: 2011-02-10
Mycophenolate Mofetil (Cellcept)
Dosage: 1 g, per day
Administration route: Oral
Start date: 2011-03-01
End date: 2011-03-08
Bactrim
Dosage: 400 mg, per day
Administration route: Oral
Start date: 2011-01-24
End date: 2011-02-01
RAD 666 / RAD 001a
Dosage: 3 mg, qd
Administration route: Oral
Indication: Renal Transplant
Start date: 2011-02-02
End date: 2011-02-09
Neoral
Dosage: 100 mg, qd
Administration route: Oral
Start date: 2011-02-27
End date: 2011-03-16
Neoral
Dosage: unk
Mycophenolate Mofetil (Cellcept)
Dosage: 2 g, per day
Administration route: Oral
Indication: Renal Transplant
Start date: 2011-01-15
End date: 2011-02-09
Neoral
Dosage: 400 mg, qd
Administration route: Oral
Indication: Renal Transplant
Start date: 2011-01-17
End date: 2011-02-01
Prednisone TAB
Dosage: 40 mg, per day
Administration route: Oral
Indication: Renal Transplant
Start date: 2011-01-16
Zantac
Dosage: 150 mg, per day
Administration route: Oral
Start date: 2011-02-02
Valganciclovir
Dosage: 250 mg, 9qd
Administration route: Oral
Start date: 2011-01-29
End date: 2011-02-01
Nexium
Dosage: 40 mg, per day
Administration route: Oral
Start date: 2011-01-16
End date: 2011-02-01
Other drugs received by patient: Solu-Medrol; Lasix; Adancor; Esomeprazole Magnesium; Calcidia; Pantoprazole; Aspirin; Sodium Bicarbonate; Amlodipine Besylate; Econazole Nitrate; Amoxicillin; Imodium; Simulect; Eprex; Insulatard NPH Human; Potassium Chloride; Nitroderm; Mirtazapine; Aluminum Hydroxide and Magnesium Trisilicate; Alfuzosin HCL; Cotrim
Possible Neoral side effects in male
Reported by a health professional (non-physician/pharmacist) from Japan on 2012-04-20
Patient: male
Reactions: Gastrointestinal Haemorrhage, Enterococcal Infection, Coagulopathy, Disseminated Intravascular Coagulation, Cardiac Failure Acute, Pneumonia Cytomegaloviral, Anal Fistula, Pneumocystis Jiroveci Pneumonia, Colonic Fistula, Circulatory Collapse, Acute Respiratory Distress Syndrome, Apnoea, Melaena, Cytomegalovirus Enterocolitis, Metabolic Acidosis, Restlessness, Gastrointestinal Ulcer Haemorrhage, Hyperglycaemia, Anaemia, Duodenal Ulcer, Ulcer, Delirium, Fungal Infection, Insomnia, Systemic Inflammatory Response Syndrome, Septic Shock, Hypoventilation, Shock Haemorrhagic, Oral Administration Complication, Ileal Ulcer, Large Intestinal Ulcer, Ileal Fistula, Interstitial Lung Disease, Small Intestinal Haemorrhage, Acute Respiratory Failure, Dyspnoea, Respiratory Failure, Diarrhoea, Sepsis, Purulence, Anal Haemorrhage, Hypertension
Adverse event resulted in: death, life threatening event
Drug(s) suspected as cause:
Bredinin
Dosage: 100 mg, daily
Administration route: Oral
End date: 2011-03-08
Prednisolone
Dosage: 10 mg, unk
End date: 2011-03-22
Prograf
Dosage: 2 mg, daily
Administration route: Oral
Start date: 2006-11-01
End date: 2011-11-17
Rituximab
Dosage: unk ukn, unk
Neoral
Dosage: 100 mg, daily
Administration route: Oral
Start date: 2010-11-18
End date: 2011-03-15
Prednisolone
Dosage: 10 mg, daily
Administration route: Oral
Start date: 2006-11-01
End date: 2011-03-18
Neoral
Dosage: 50 mg, daily
Administration route: Oral
Indication: Renal Transplant
Start date: 2010-11-18
End date: 2011-03-15
Other drugs received by patient: Insulin
Possible Neoral side effects in 79 year old female
Reported by a physician from Japan on 2012-04-18
Patient: 79 year old female
Reactions: Disseminated Intravascular Coagulation, Urinary Tract Infection, Sepsis, Platelet Count Decreased, Urinary Retention
Adverse event resulted in: life threatening event
Drug(s) suspected as cause:
Neoral
Dosage: 150 mg/ daily
Administration route: Oral
Start date: 2011-07-06
End date: 2011-08-08
Neoral
Dosage: 100 mg,daily
Administration route: Oral
Start date: 2011-08-09
Neoral
Dosage: 100 mg/ daily
Administration route: Oral
Indication: Mixed Connective Tissue Disease
Start date: 2011-06-28
End date: 2011-07-05
Possible Neoral side effects in female
Reported by a physician from United States on 2012-04-11
Patient: female, weighing 59.0 kg (129.8 pounds)
Reactions: Death, Arterial Thrombosis, Myocardial Infarction
Adverse event resulted in: death, life threatening event, hospitalization
Drug(s) suspected as cause:
Neoral
Other drugs received by patient: Heparin; Inderal; Hydrocortisone; Carafate; Nahco3 (Sodium Bicarbonate); Flagyl; Ativan; Regular Humulin Insulin (Insulin Human); Urokinase; Nitroglycerin; Dopamine HCL
Possible Neoral side effects in female
Reported by a physician from United States on 2012-04-11
Patient: female, weighing 50.0 kg (110.0 pounds)
Reactions: Death, Ventricular Tachycardia, Transplant Rejection, Myocardial Infarction
Adverse event resulted in: death, life threatening event, hospitalization
Drug(s) suspected as cause:
Neoral
Other drugs received by patient: Procardia; Mycostatin; Ceftriaxone; Acyclovir; MVI (Multivitamins); Colace (Docusate Sodium); Zantac; Bactrim SS (Bactrim); Lasix
Possible Neoral side effects in female
Reported by a health professional (non-physician/pharmacist) from Norway on 2012-04-09
Patient: female
Reactions: Night Sweats, Weight Decreased, Anaplastic Large Cell Lymphoma T- and Null-Cell Types Stage IV, Lung Disorder, Pleural Effusion, Pyrexia, Abdominal Pain Upper
Adverse event resulted in: life threatening event, hospitalization
Drug(s) suspected as cause:
Neoral
Dosage: 100 mg, bid
Administration route: Oral
Indication: Behcet's Syndrome
Start date: 2008-10-01
End date: 2009-09-25
Imuran
Dosage: 50 mg, bid
Administration route: Oral
Indication: Behcet's Syndrome
Start date: 2009-09-25
End date: 2011-11-08
Remicade
Dosage: 300 mg, unk
Indication: Behcet's Syndrome
Start date: 2010-03-19
End date: 2011-11-08
Other drugs received by patient: Prednisolone; Calcigran Forte; Paralgin Forte; Alendronic Acid
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