MYFORTIC Side Effects

7009498-6 | Volvulus
on Sep 13, 2010 Female patient from UNITED STATES , 43 years of age, was diagnosed with renal transplant and was treated with Myfortic (View Usage). Patient experienced the following unwanted or unexpected effects: volvulus. Myfortic dosage: 720 Mg Daily. During the same period patient was treated with PROGRAF (3 Mg, Unk) (View Prograf Review and Prograf Label ). Patient was hospitalized.

7007990-1 | Asthenia, Blood Creatinine Increased, Diarrhoea, Haemodialysis, Nervous System Disorder, Urine Output Decreased
Patient was taking Myfortic (View Usage). Patient had the following side effects: asthenia, blood creatinine increased, diarrhoea, haemodialysis, nervous system disorder, urine output decreased on Sep 09, 2010 from POLAND Additional patient health information: Male patient , weighting 154.3 lb, was diagnosed with renal transplant and. Myfortic dosage: 1440 Mg. During the same period patient was treated with TACROLIMUS (11 Mg/24 Hours) (View Tacrolimus Review and Tacrolimus Label ), ENCORTON (20 Mg) (View Encorton Review and Encorton Label ), CERTICAN (1.5 Mg/day) (View Certican Review and Certican Label ), SANDIMMUNE (View Sandimmune Review and Sandimmune Label ), CYCLOSPORINE (View Cyclosporine Review and Cyclosporine Label ). Patient was hospitalized.

6968790-1 | Retroperitoneal Haematoma, Spinal Cord Herniation, Surgery
Adverse event was reported on Sep 01, 2010 by a Female patient taking Myfortic (View Usage) (Dosage: 360 3-0-3) was diagnosed with renal transplant and. Location: GERMANY , weighting 205.0 lb, After Myfortic was administered, patient had the following side effects: retroperitoneal haematoma, spinal cord herniation, surgery (What is surgery?). During the same period patient was treated with SANDIMMUNE (View Sandimmune Review and Sandimmune Label ), NO TREATMENT RECEIVED NOMED (View No Treatment Received Nomed Review and No Treatment Received Nomed Label ), URBASON (4-0-0) (View Urbason Review and Urbason Label ). Patient was hospitalized.

6968470-2 | Colitis Ulcerative, Diarrhoea, Renal Failure Acute, Weight Decreased
on Aug 31, 2010 Male patient from FRANCE , weighting 132.3 lb, was diagnosed with renal transplant and was treated with Myfortic (View Usage). Patient experienced the following unwanted or unexpected effects: colitis ulcerative, diarrhoea, renal failure acute, weight decreased. Myfortic dosage: 720 Mg / Day. During the same period patient was treated with CERTICAN (3 Mg / Day) (View Certican Review and Certican Label ), NEORAL (Unk) (View Neoral Review and Neoral Label ), AUGMENTIN '125' (View Augmentin '125' Review and Augmentin '125' Label ), CORTANCYL (View Cortancyl Review and Cortancyl Label ), ROVALCYTE (View Rovalcyte Review and Rovalcyte Label ). Patient was hospitalized.


6966361-4 | Retroperitoneal Haematoma, Spinal Cord Herniation, Surgery
on Aug 30, 2010 Female patient from GERMANY , weighting 205.0 lb, was diagnosed with renal transplant and was treated with Myfortic (View Usage). Patient had the following side effects: retroperitoneal haematoma, spinal cord herniation, surgery (What is surgery?). Myfortic dosage: 360 3-0-3. During the same period patient was treated with SANDIMMUNE (View Sandimmune Review and Sandimmune Label ), NO TREATMENT RECEIVED NOMED (View No Treatment Received Nomed Review and No Treatment Received Nomed Label ), URBASON (4-0-0) (View Urbason Review and Urbason Label ). Patient was hospitalized.

6956995-5 | Grand Mal Convulsion, Headache, Hyperhidrosis, Hypertension, Nausea
Patient was taking Myfortic (View Usage). After Myfortic was administered, patient had the following side effects: grand mal convulsion, headache (What is headache?), hyperhidrosis, hypertension, nausea (What is nausea?) on Aug 27, 2010 from UNITED STATES Additional patient health information: Female patient , weighting 86.99 lb, was diagnosed with immunosuppression, nausea (What is nausea?) and. Myfortic dosage: 720 Mg Bid Po. During the same period patient was treated with PROGRAF (View Prograf Review and Prograf Label ), PREDNISONE (View Prednisone Review and Prednisone Label ), VALCYTE (View Valcyte Review and Valcyte Label ), SPORANOX (View Sporanox Review and Sporanox Label ), BACTRIM DS (View Bactrim Ds Review and Bactrim Ds Label ), NYSTATIN ORAL SUSPENSION (View Nystatin Oral Suspension Review and Nystatin Oral Suspension Label ), ZYRTEC (View Zyrtec Review and Zyrtec Label ). Patient was hospitalized.

6955298-2 | Cerebrovascular Accident, Dysphagia
Adverse event was reported on Aug 17, 2010 by a Female patient taking Myfortic (View Usage) (Dosage: 180 Mg, Bid) was diagnosed with renal transplant and. Location: GERMANY , 72 years of age, Patient experienced the following unwanted or unexpected effects: cerebrovascular accident, dysphagia. Patient was hospitalized.

6940266-7 | Decreased Appetite, Fatigue, Forced Expiratory Volume Abnormal, Pain, Tremor, Wheezing
on Aug 11, 2010 Female patient from BELGIUM , 32 years of age, was diagnosed with lung transplant (What is lung transplant?), pulmonary function test decreased and was treated with Myfortic (View Usage). Patient had the following side effects: decreased appetite, fatigue, forced expiratory volume abnormal, pain (What is pain?), tremor, wheezing. Myfortic dosage: Unk. During the same period patient was treated with PROGRAFT (Unk) (View Prograft Review and Prograft Label ), CORTICOSTEROIDS (Unk) (View Corticosteroids Review and Corticosteroids Label ), PANCREATIC ENZYMES (Unk) (View Pancreatic Enzymes Review and Pancreatic Enzymes Label ).

6935316-8 | Blood Creatinine Increased, C-reactive Protein Increased, Cyst Drainage, Lymphocele, Proteus Infection, Seroma, Therapeutic Procedure, Ureteric Obstruction, Urethritis
on Aug 11, 2010 Male patient from GERMANY , weighting 169.8 lb, was diagnosed with renal transplant and was treated with Myfortic (View Usage). After Myfortic was administered, patient had the following side effects: blood creatinine increased, c-reactive protein increased, cyst drainage, lymphocele, proteus infection, seroma, therapeutic procedure, ureteric obstruction, urethritis. Myfortic dosage: 720 Mg, Bid. During the same period patient was treated with NEORAL (250 Mg, Bid) (View Neoral Review and Neoral Label ), PREDNISOLONE (20 Mg, Qd) (View Prednisolone Review and Prednisolone Label ), NO TREATMENT RECEIVED NOMED (No Treatment) (View No Treatment Received Nomed Review and No Treatment Received Nomed Label ). Patient was hospitalized.

6935315-6 | Blood Creatinine Increased, C-reactive Protein Increased, Cyst Drainage, Lymphocele, Proteus Infection, Seroma, Therapeutic Procedure, Ureteric Obstruction, Urethritis
Patient was taking Myfortic (View Usage). Patient experienced the following unwanted or unexpected effects: blood creatinine increased, c-reactive protein increased, cyst drainage, lymphocele, proteus infection, seroma, therapeutic procedure, ureteric obstruction, urethritis on Aug 11, 2010 from GERMANY Additional patient health information: Male patient , weighting 169.8 lb, was diagnosed with renal transplant and. Myfortic dosage: 720 Mg, Bid. During the same period patient was treated with NEORAL (250 Mg, Bid) (View Neoral Review and Neoral Label ), PREDNISOLONE (20 Mg, Qd) (View Prednisolone Review and Prednisolone Label ), NO TREATMENT RECEIVED NOMED (No Treatment) (View No Treatment Received Nomed Review and No Treatment Received Nomed Label ). Patient was hospitalized.

6930963-1 | Anaemia, Kidney Transplant Rejection, Leukopenia, Proteinuria
Adverse event was reported on Aug 17, 2010 by a Female patient taking Myfortic (View Usage) (Dosage: 360 Mg Daily Twice Daily) was diagnosed with immunosuppression and. Location: UNITED STATES , 61 years of age, weighting 176.4 lb, Patient had the following side effects: anaemia, kidney transplant rejection, leukopenia, proteinuria. During the same period patient was treated with TACROLIMUS (View Tacrolimus Review and Tacrolimus Label ), PREDNISONE (View Prednisone Review and Prednisone Label ). Patient was hospitalized.

6923323-0 | Blood Creatinine Increased, Complications Of Transplanted Kidney, Concomitant Disease Progression, Lymphocele, Pneumonia, Renal Failure Acute, Ureteral Stent Insertion, Ureteric Stenosis
on Aug 06, 2010 Male patient from GERMANY , weighting 180.3 lb, was diagnosed with renal transplant and was treated with Myfortic (View Usage). After Myfortic was administered, patient had the following side effects: blood creatinine increased, complications of transplanted kidney, concomitant disease progression, lymphocele, pneumonia (What is pneumonia?), renal failure acute, ureteral stent insertion, ureteric stenosis. Myfortic dosage: 720mg Daily. During the same period patient was treated with SANDIMMUNE (200mg Daily) (View Sandimmune Review and Sandimmune Label ), NO TREATMENT RECEIVED NOMED (No Treatment) (View No Treatment Received Nomed Review and No Treatment Received Nomed Label ), DECORTIN (5 Mg) (View Decortin Review and Decortin Label ). Patient was hospitalized.

6919082-8 | Colitis Ulcerative, Diarrhoea, Renal Failure Acute, Weight Decreased
on Aug 03, 2010 Male patient from FRANCE , weighting 132.3 lb, was diagnosed with renal transplant and was treated with Myfortic (View Usage). Patient experienced the following unwanted or unexpected effects: colitis ulcerative, diarrhoea, renal failure acute, weight decreased. Myfortic dosage: 720 Mg / Day. During the same period patient was treated with CERTICAN (3 Mg / Day) (View Certican Review and Certican Label ), NEORAL (Unk) (View Neoral Review and Neoral Label ), AUGMENTIN '125' (View Augmentin '125' Review and Augmentin '125' Label ), CORTANCYL (View Cortancyl Review and Cortancyl Label ), ROVALCYTE (View Rovalcyte Review and Rovalcyte Label ). Patient was hospitalized.

6909329-6 | Blood Glucose Increased, Diabetes Mellitus Inadequate Control, Glycosylated Haemoglobin Increased
Patient was taking Myfortic (View Usage). Patient had the following side effects: blood glucose increased, diabetes mellitus inadequate control, glycosylated haemoglobin increased on Jul 28, 2010 from GERMANY Additional patient health information: Female patient , weighting 213.8 lb, was diagnosed with renal transplant and. Myfortic dosage: 720 Unk, Bid. During the same period patient was treated with SIMULECT (20 Unk, Qd) (View Simulect Review and Simulect Label ), SANDIMMUNE (100 Unk, Bid) (View Sandimmune Review and Sandimmune Label ), CORTICOSTEROIDS (View Corticosteroids Review and Corticosteroids Label ), NO TREATMENT RECEIVED NOMED (View No Treatment Received Nomed Review and No Treatment Received Nomed Label ). Patient was hospitalized.

6900002-7 | Blood Creatinine Increased, Complications Of Transplanted Kidney, Concomitant Disease Progression, Lymphocele, Pneumonia, Renal Failure Acute, Ureteral Stent Insertion, Ureteric Stenosis
Adverse event was reported on Jul 19, 2010 by a Male patient taking Myfortic (View Usage) (Dosage: 720mg Daily) was diagnosed with renal transplant and. Location: GERMANY , weighting 180.3 lb, After Myfortic was administered, patient had the following side effects: blood creatinine increased, complications of transplanted kidney, concomitant disease progression, lymphocele, pneumonia (What is pneumonia?), renal failure acute, ureteral stent insertion, ureteric stenosis. During the same period patient was treated with SANDIMMUNE (200mg Daily) (View Sandimmune Review and Sandimmune Label ), NO TREATMENT RECEIVED NOMED (No Treatment) (View No Treatment Received Nomed Review and No Treatment Received Nomed Label ), DECORTIN (5 Mg) (View Decortin Review and Decortin Label ). Patient was hospitalized.

6894624-X | Adhesiolysis, Bacteraemia, Candidiasis, Cardiogenic Shock, Confusional State, Dialysis, Enterococcal Infection, Ileus, Klebsiella Infection
on Jul 21, 2010 Male patient from SWITZERLAND , 60 years of age, was diagnosed with immunosuppression, renal transplant and was treated with Myfortic (View Usage). Patient experienced the following unwanted or unexpected effects: adhesiolysis, bacteraemia, candidiasis, cardiogenic shock, confusional state, dialysis (What is dialysis?), enterococcal infection, ileus, klebsiella infection. Myfortic dosage: Unk. During the same period patient was treated with TACROLIMUS (Unk) (View Tacrolimus Review and Tacrolimus Label ), IMUREK (Unk) (View Imurek Review and Imurek Label ). Patient was hospitalized.

6878855-0 | Blood Creatinine Increased, Complications Of Transplanted Kidney, Concomitant Disease Progression, Lymphocele, Pneumonia, Renal Failure Acute, Ureteral Stent Insertion, Ureteric Stenosis
on Jul 19, 2010 Male patient from GERMANY , weighting 180.3 lb, was diagnosed with renal transplant and was treated with Myfortic (View Usage). Patient had the following side effects: blood creatinine increased, complications of transplanted kidney, concomitant disease progression, lymphocele, pneumonia (What is pneumonia?), renal failure acute, ureteral stent insertion, ureteric stenosis. Myfortic dosage: 720mg Daily. During the same period patient was treated with SANDIMMUNE (200mg Daily) (View Sandimmune Review and Sandimmune Label ), NO TREATMENT RECEIVED NOMED (No Treatment) (View No Treatment Received Nomed Review and No Treatment Received Nomed Label ), DECORTIN (5 Mg) (View Decortin Review and Decortin Label ). Patient was hospitalized.

6861992-4 | Gastritis, H1n1 Influenza, Kidney Transplant Rejection, Renal Transplant
Patient was taking Myfortic (View Usage). After Myfortic was administered, patient had the following side effects: gastritis, h1n1 influenza, kidney transplant rejection, renal transplant on Jul 06, 2010 from UNITED STATES Additional patient health information: Female patient , child 9 years of age, weighting 22.05 lb, was diagnosed with renal transplant, prophylaxis against transplant rejection, hypertension, proteinuria, blood iron decreased, blood pressure (What is blood pressure?), magnesium deficiency, oedema and. Myfortic dosage: 360 Mg, Daily. During the same period patient was treated with ENALAPRIL MALEATE (5 Mg, Daily) (View Enalapril Maleate Review and Enalapril Maleate Label ), HECTOROL (2 Ug, Daily) (View Hectorol Review and Hectorol Label ), NIFEDIPINE (10 Mg, Prn) (View Nifedipine Review and Nifedipine Label ), IRON (300 Mg, Daily) (View Iron Review and Iron Label ), MAGNESIUM OXIDE (800 Mg, Daily) (View Magnesium Oxide Review and Magnesium Oxide Label ), LASIX (20 Mg, Daily) (View Lasix Review and Lasix Label ). Patient was hospitalized.

6841181-X | Ankle Fracture, Pyrexia
Adverse event was reported on Jul 05, 2010 by a Female patient taking Myfortic (View Usage) (Dosage: 1440 Mg, Daily) was diagnosed with renal and pancreas transplant, prophylaxis against transplant rejection and. Location: UNITED STATES , 39 years of age, Patient experienced the following unwanted or unexpected effects: ankle fracture, pyrexia. During the same period patient was treated with PROGRAF (8 Mg, Daily) (View Prograf Review and Prograf Label ). Patient was hospitalized.

6831534-8 | Blood Pressure Decreased, Diarrhoea, Haemorrhage, Memory Impairment, Normochromic Normocytic Anaemia, Psychomotor Skills Impaired, Renal Failure Acute, Urinary Tract Infection
on Jun 28, 2010 Male patient from FRANCE , weighting 154.3 lb, was diagnosed with liver transplant (What is liver transplant?) and was treated with Myfortic (View Usage). Patient had the following side effects: blood pressure decreased, diarrhoea, haemorrhage, memory impairment, normochromic normocytic anaemia, psychomotor skills impaired, renal failure acute, urinary tract infection (What is urinary tract infection?). Myfortic dosage: 360 Mg, Bid. During the same period patient was treated with TRIATEC (5 Mg/day) (View Triatec Review and Triatec Label ), LASIX (40 Mg/day) (View Lasix Review and Lasix Label ), TARDYFERON (2 Df/day) (View Tardyferon Review and Tardyferon Label ), SODIUM BICARBONATE (1 G, Unk) (View Sodium Bicarbonate Review and Sodium Bicarbonate Label ), EUPRESSYL (60 Mg, Tid) (View Eupressyl Review and Eupressyl Label ). Patient was hospitalized.

6830752-2 | Food Poisoning
on Jun 28, 2010 Male patient from UNITED STATES , 55 years of age, was diagnosed with prophylaxis against transplant rejection, liver transplant (What is liver transplant?), ulcer (What is ulcer?), cholecystectomy, blood pressure (What is blood pressure?), cytomegalovirus infection (What is cytomegalovirus infection?), insomnia and was treated with Myfortic (View Usage). After Myfortic was administered, patient had the following side effects: food poisoning. Myfortic dosage: 720 Mg, Daily. During the same period patient was treated with PROGRAF (4 Mg, Daily) (View Prograf Review and Prograf Label ), PROTONIX (40 Mg, Daily) (View Protonix Review and Protonix Label ), ASPIRIN (81 Mg, Daily) (View Aspirin Review and Aspirin Label ), ACTIGALL (600 Mg, Daily) (View Actigall Review and Actigall Label ), COZAAR (25 Mg, Daily) (View Cozaar Review and Cozaar Label ), SEPTRA (3 X 400 Mg-80 Mg,weekly) (View Septra Review and Septra Label ), AMBIEN (10 Mg, Daily) (View Ambien Review and Ambien Label ). Patient was hospitalized.

6826302-7 | Abdominal Pain, Anaemia, Cytomegalovirus Infection, Diarrhoea, Granulocytopenia, Malaise, Pyrexia, White Blood Cell Count Decreased
Patient was taking Myfortic (View Usage). Patient experienced the following unwanted or unexpected effects: abdominal pain (What is abdominal pain?), anaemia, cytomegalovirus infection (What is cytomegalovirus infection?), diarrhoea, granulocytopenia, malaise, pyrexia, white blood cell count decreased on Jun 30, 2010 from UNITED STATES Additional patient health information: Male patient , weighting 167.6 lb, was diagnosed with renal transplant and. Myfortic dosage: 720 Mg, Bid. During the same period patient was treated with PREDNISONE (15 Mg, Qd) (View Prednisone Review and Prednisone Label ), MYCOPHENOLATE MOFETIL (Unk) (View Mycophenolate Mofetil Review and Mycophenolate Mofetil Label ), GANCICLOVIR (View Ganciclovir Review and Ganciclovir Label ), ATENOLOL (View Atenolol Review and Atenolol Label ). Patient was hospitalized.

6814979-1 | Clumsiness, Fall, Motor Dysfunction, Movement Disorder, Muscular Weakness, Speech Disorder, Walking Aid User
Adverse event was reported on Jun 30, 2010 by a Female patient taking Myfortic (View Usage) (Dosage: ) . Location: UNITED STATES , 47 years of age, weighting 165.0 lb, Patient had the following side effects: clumsiness, fall (What is fall?), motor dysfunction, movement disorder (What is movement disorder?), muscular weakness, speech disorder, walking aid user. During the same period patient was treated with CELLCEPT (View Cellcept Review and Cellcept Label ). Patient was hospitalized.

6814021-2 | Blood Glucose Increased, Diabetes Mellitus Inadequate Control, Glycosylated Haemoglobin Increased
on Jun 21, 2010 Female patient from GERMANY , weighting 213.8 lb, was diagnosed with renal transplant and was treated with Myfortic (View Usage). After Myfortic was administered, patient had the following side effects: blood glucose increased, diabetes mellitus inadequate control, glycosylated haemoglobin increased. Myfortic dosage: 720 Unk, Bid. During the same period patient was treated with SIMULECT (20 Unk, Qd) (View Simulect Review and Simulect Label ), SANDIMMUNE (100 Unk, Bid) (View Sandimmune Review and Sandimmune Label ), NO TREATMENT RECEIVED NOMED (View No Treatment Received Nomed Review and No Treatment Received Nomed Label ). Patient was hospitalized.

6813379-8 | Coagulopathy, Confusional State, Disorientation, Hallucination, Visual, Post Procedural Haemorrhage
on Jun 24, 2010 Male patient from SPAIN , weighting 154.3 lb, was diagnosed with renal transplant and was treated with Myfortic (View Usage). Patient experienced the following unwanted or unexpected effects: coagulopathy, confusional state, disorientation, hallucination, visual, post procedural haemorrhage. Myfortic dosage: 1440 Mg. During the same period patient was treated with TACROLIMUS (10 Mg) (View Tacrolimus Review and Tacrolimus Label ). Patient was hospitalized.

6783404-1 | Aplastic Anaemia, Normochromic Normocytic Anaemia
Patient was taking Myfortic (View Usage). Patient had the following side effects: aplastic anaemia, normochromic normocytic anaemia on Jun 15, 2010 from UNITED STATES Additional patient health information: Male patient , weighting 130.1 lb, . Myfortic dosage: 360 Mg, Bid. During the same period patient was treated with NEORAL (View Neoral Review and Neoral Label ), PREDNISONE (View Prednisone Review and Prednisone Label ), CLINDAMYCIN (View Clindamycin Review and Clindamycin Label ), LISINOPRIL (View Lisinopril Review and Lisinopril Label ), FISH OIL (View Fish Oil Review and Fish Oil Label ).

6780191-8 | Herpes Zoster, Micturition Disorder, Pain, Rash, Skin Lesion
Adverse event was reported on Jun 11, 2010 by a Male patient taking Myfortic (View Usage) (Dosage: Unk) was diagnosed with renal transplant and. Location: SPAIN , weighting 381.4 lb, After Myfortic was administered, patient had the following side effects: herpes zoster, micturition disorder, pain (What is pain?), rash (What is rash?), skin lesion. During the same period patient was treated with TACROLIMUS (2.5mg/day) (View Tacrolimus Review and Tacrolimus Label ). Patient was hospitalized.

6774496-4 | Apoptosis, Colitis, Diarrhoea, Gastrointestinal Toxicity, Inflammatory Bowel Disease, Metaplasia, Polyglandular Disorder
on Jun 08, 2010 Female patient from UNITED STATES , 14 years of age, was diagnosed with immunosuppression and was treated with Myfortic (View Usage). Patient experienced the following unwanted or unexpected effects: apoptosis, colitis, diarrhoea, gastrointestinal toxicity, inflammatory bowel disease, metaplasia, polyglandular disorder. Myfortic dosage: 360 Mg, Bid. During the same period patient was treated with AZATHIOPRINE (View Azathioprine Review and Azathioprine Label ). Patient was hospitalized.

6774494-0 | Apoptosis, Diarrhoea, Gastrointestinal Injury, Iron Deficiency Anaemia, Weight Decreased
on Jun 08, 2010 Male patient from UNITED STATES , 52 years of age, weighting 153.2 lb, was treated with Myfortic (View Usage). Patient had the following side effects: apoptosis, diarrhoea, gastrointestinal injury, iron deficiency anaemia, weight decreased. Myfortic dosage: 360 Mg, Bid. Patient was hospitalized.

6770572-0 | Bladder Dilatation, Bladder Spasm, Blood Pressure Abnormal, Chills, Device Malfunction, Enterococcal Infection, Fatigue, Hydronephrosis, Pyrexia
Patient was taking Myfortic (View Usage). After Myfortic was administered, patient had the following side effects: bladder dilatation, bladder spasm, blood pressure abnormal, chills, device malfunction, enterococcal infection, fatigue, hydronephrosis, pyrexia on Jun 07, 2010 from UNITED STATES Additional patient health information: Male patient , 51 years of age, weighting 188.7 lb, was diagnosed with renal transplant and. Myfortic dosage: 540 Mg, Qd. During the same period patient was treated with PREDNISOLONE (5 Mg, Qd) (View Prednisolone Review and Prednisolone Label ), SEPTRA (View Septra Review and Septra Label ), VALCYTE (View Valcyte Review and Valcyte Label ), PREVACID (View Prevacid Review and Prevacid Label ), PANCREASE (View Pancrease Review and Pancrease Label ), ASPIRIN (View Aspirin Review and Aspirin Label ), LIPITOR (View Lipitor Review and Lipitor Label ), SENSIPAR (View Sensipar Review and Sensipar Label ). Patient was hospitalized.

6759101-5 | Herpes Zoster, Micturition Disorder, Pain, Rash, Skin Lesion
Adverse event was reported on May 25, 2010 by a Male patient taking Myfortic (View Usage) (Dosage: Unk) was diagnosed with renal transplant and. Location: SPAIN , weighting 381.4 lb, Patient experienced the following unwanted or unexpected effects: herpes zoster, micturition disorder, pain (What is pain?), rash (What is rash?), skin lesion. During the same period patient was treated with TACROLIMUS (2.5mg/day) (View Tacrolimus Review and Tacrolimus Label ). Patient was hospitalized.

6758863-0 | Knee Arthroplasty
on May 23, 2010 Female patient from UNITED STATES , 48 years of age, was diagnosed with prophylaxis against transplant rejection and was treated with Myfortic (View Usage). Patient had the following side effects: knee arthroplasty. Myfortic dosage: 250 Mg Daily. During the same period patient was treated with METHYLPREDNISOLONE (5 Daily) (View Methylprednisolone Review and Methylprednisolone Label ), PROGRAF (14 Mg, Daily) (View Prograf Review and Prograf Label ). Patient was hospitalized.

6750083-9 | Device Related Infection
on May 27, 2010 Female patient from UNITED STATES , 49 years of age, weighting 171.0 lb, was treated with Myfortic (View Usage). After Myfortic was administered, patient had the following side effects: device related infection. Myfortic dosage: . During the same period patient was treated with PROGRAF (View Prograf Review and Prograf Label ), PREDNISONE (View Prednisone Review and Prednisone Label ), NYSTATIN ORAL SUSPENSION (View Nystatin Oral Suspension Review and Nystatin Oral Suspension Label ), AZITHROMYCIN (View Azithromycin Review and Azithromycin Label ), BENZONATATE (View Benzonatate Review and Benzonatate Label ), TESSALON (View Tessalon Review and Tessalon Label ), NOVOLOG (View Novolog Review and Novolog Label ), EPOETIN ALPHA INJ (View Epoetin Alpha Inj Review and Epoetin Alpha Inj Label ). Patient was hospitalized.

6749004-4 | Impaired Healing, Wound Treatment
Patient was taking Myfortic (View Usage). Patient experienced the following unwanted or unexpected effects: impaired healing, wound treatment on May 25, 2010 from GERMANY Additional patient health information: Male patient , weighting 223.8 lb, was diagnosed with renal transplant and. Myfortic dosage: 1440mg, Daily. During the same period patient was treated with NO TREATMENT RECEIVED NOMED (Unk) (View No Treatment Received Nomed Review and No Treatment Received Nomed Label ), SANDIMMUNE (200mg, Daily) (View Sandimmune Review and Sandimmune Label ), PREDNISONE TAB (15mg, Daily) (View Prednisone Tab Review and Prednisone Tab Label ). Patient was hospitalized.

6739856-6 | Ocular Vasculitis, Renal Lymphocele, Uveitis, Visual Acuity Reduced
Adverse event was reported on May 18, 2010 by a Male patient taking Myfortic (View Usage) (Dosage: 720 Mg, Bid) was diagnosed with renal transplant and. Location: GERMANY , weighting 176.4 lb, Patient had the following side effects: ocular vasculitis, renal lymphocele, uveitis, visual acuity reduced. During the same period patient was treated with SANDIMMUNE (100 Mg, Bid) (View Sandimmune Review and Sandimmune Label ), NO TREATMENT RECEIVED NOMED (Unk) (View No Treatment Received Nomed Review and No Treatment Received Nomed Label ), DECORTIN H (12.5 Mg / Day) (View Decortin-h Review and Decortin-h Label ). Patient was hospitalized.

6729689-9 | Aplastic Anaemia, Normochromic Normocytic Anaemia
on May 11, 2010 Male patient from UNITED STATES , weighting 130.1 lb, was treated with Myfortic (View Usage). After Myfortic was administered, patient had the following side effects: aplastic anaemia, normochromic normocytic anaemia. Myfortic dosage: 360 Mg, Bid. During the same period patient was treated with NEORAL (View Neoral Review and Neoral Label ), PREDNISONE (View Prednisone Review and Prednisone Label ), CLINDAMYCIN (View Clindamycin Review and Clindamycin Label ), LISINOPRIL (View Lisinopril Review and Lisinopril Label ), FISH OIL (View Fish Oil Review and Fish Oil Label ).

6725475-4 | Asthenia, Chills, Decreased Appetite, Oedema Peripheral, Pain In Extremity, Peripheral Coldness, Skin Disorder, Tremor
on May 13, 2010 Male patient from UNITED STATES , 66 years of age, weighting 140.0 lb, was treated with Myfortic (View Usage). Patient experienced the following unwanted or unexpected effects: asthenia, chills, decreased appetite, oedema peripheral, pain in extremity, peripheral coldness, skin disorder, tremor. Myfortic dosage: 360 Mg X 2 Am Pm Daily 720 Mg X 2 Am Pm Daily. Patient was hospitalized.

6721592-3 | Amnesia
Patient was taking Myfortic (View Usage). Patient had the following side effects: amnesia on Apr 19, 2010 from UNITED STATES Additional patient health information: Male patient , 53 years of age, weighting 187.4 lb, was diagnosed with liver transplant (What is liver transplant?), immunosuppression, cholecystectomy, hypertension, insomnia and. Myfortic dosage: Unk. During the same period patient was treated with PROGRAF (View Prograf Review and Prograf Label ), PROTONIX (View Protonix Review and Protonix Label ), ACTIGALL (View Actigall Review and Actigall Label ), COZAAR (View Cozaar Review and Cozaar Label ), ASPIRIN (81 Mg/day) (View Aspirin Review and Aspirin Label ), AMBIEN (10 Mg/day) (View Ambien Review and Ambien Label ).

6714022-9 | Epistaxis, Loss Of Consciousness
Adverse event was reported on Apr 26, 2010 by a Female patient taking Myfortic (View Usage) (Dosage: ) . Location: CANADA , 17 years of age, After Myfortic was administered, patient had the following side effects: epistaxis, loss of consciousness. During the same period patient was treated with CELEXA (10 Mg) (View Celexa Review and Celexa Label ).

6700934-9 | Neutropenia
on Apr 20, 2010 Female patient from BELGIUM , weighting 158.7 lb, was diagnosed with renal transplant and was treated with Myfortic (View Usage). Patient experienced the following unwanted or unexpected effects: neutropenia. Myfortic dosage: 720 Mg / Day. During the same period patient was treated with NEORAL (135 Mg / Day) (View Neoral Review and Neoral Label ), NO TREATMENT RECEIVED NOMED (Unk) (View No Treatment Received Nomed Review and No Treatment Received Nomed Label ), METHYLPREDNISOLONE (4 Mg / Day) (View Methylprednisolone Review and Methylprednisolone Label ), COTRIM (View Cotrim Review and Cotrim Label ). Patient was hospitalized.

6695201-6 | Gastritis, H1n1 Influenza, Transplant Rejection
on Mar 25, 2010 Female patient from UNITED STATES , child 9 years of age, was diagnosed with blood pressure (What is blood pressure?), blood iron decreased, hypertension, oedema, immunosuppression, anaemia and was treated with Myfortic (View Usage). Patient had the following side effects: gastritis, h1n1 influenza, transplant rejection. Myfortic dosage: 360 Mg, Daily. During the same period patient was treated with ENALAPRIL MALEATE (5 Mg Daily) (View Enalapril Maleate Review and Enalapril Maleate Label ), HECTOROL (2 Ug, Daily) (View Hectorol Review and Hectorol Label ), NIFEDIPINE (10 Mg As Needed) (View Nifedipine Review and Nifedipine Label ), NU IRON 150 (300 Mg, Daily) (View Nu-iron 150 Review and Nu-iron 150 Label ), LASIX (20 Mg, Daily) (View Lasix Review and Lasix Label ), PREDNISONE (5 Mg, Daily) (View Prednisone Review and Prednisone Label ), EPOGEN (4000 U, Unk) (View Epogen Review and Epogen Label ), LIPITOR (20 Mg, Daily) (View Lipitor Review and Lipitor Label ). Patient was hospitalized.

6688364-X | Bladder Spasm, Blood Pressure Abnormal, Chills, Enterococcal Infection, Fatigue, Pyrexia, Renal Failure Acute, Tachycardia, Urinary Incontinence
Patient was taking Myfortic (View Usage). After Myfortic was administered, patient had the following side effects: bladder spasm, blood pressure abnormal, chills, enterococcal infection, fatigue, pyrexia, renal failure acute, tachycardia, urinary incontinence (What is urinary incontinence?) on Apr 09, 2010 from UNITED STATES Additional patient health information: Male patient , 51 years of age, . Myfortic dosage: . During the same period patient was treated with PREDNISOLONE (View Prednisolone Review and Prednisolone Label ). Patient was hospitalized.

6686947-4 | Amnesia
Adverse event was reported on Apr 08, 2010 by a Male patient taking Myfortic (View Usage) (Dosage: ) was diagnosed with liver transplant (What is liver transplant?), immunosuppression, cholecystectomy, hypertension and. Location: UNITED STATES , 53 years of age, weighting 187.4 lb, Patient experienced the following unwanted or unexpected effects: amnesia. During the same period patient was treated with PROGRAF (View Prograf Review and Prograf Label ), PROTONIX (View Protonix Review and Protonix Label ), ACTIGALL (View Actigall Review and Actigall Label ), COZAAR (View Cozaar Review and Cozaar Label ).

6686176-4 | Gastric Ulcer Perforation, Intestinal Ulcer Perforation
on Apr 13, 2010 Male patient from RUSSIAN FEDERATION , 52 years of age, was treated with Myfortic (View Usage). Patient had the following side effects: gastric ulcer perforation, intestinal ulcer perforation. Myfortic dosage: .

6681813-2 | Renal Disorder
on Mar 05, 2010 Female patient from UNITED STATES , 42 years of age, was diagnosed with renal transplant, immunosuppression, depression (What is depression?), gastrooesophageal reflux disease, blood cholesterol increased, angiopathy and was treated with Myfortic (View Usage). After Myfortic was administered, patient had the following side effects: renal disorder. Myfortic dosage: 1440 Mg/day. During the same period patient was treated with PREDNISOLONE (5 Mg Daily) (View Prednisolone Review and Prednisolone Label ), FLUOXETINE (20 Mg Daily) (View Fluoxetine Review and Fluoxetine Label ), OMEPRAZOLE (40 Mg Daily) (View Omeprazole Review and Omeprazole Label ), CRESTOR (5 Mg Daily) (View Crestor Review and Crestor Label ), ASPIRIN (81 Mg Daily) (View Aspirin Review and Aspirin Label ), PROGRAF (5 Mg Daily) (View Prograf Review and Prograf Label ). Patient was hospitalized.

6676604-2 | Headache, Lumbar Puncture
Patient was taking Myfortic (View Usage). Patient experienced the following unwanted or unexpected effects: headache (What is headache?), lumbar puncture on Mar 06, 2010 from UNITED STATES Additional patient health information: Female patient , 21 years of age, was diagnosed with immunosuppression, insomnia, blood cholesterol increased, graft versus host disease and. Myfortic dosage: 720 Mg Daily. During the same period patient was treated with PROGRAF (10 Mg Daily) (View Prograf Review and Prograf Label ), AMBIEN (10mg Daily) (View Ambien Review and Ambien Label ), PRAVACHOL (40 Mg Daily) (View Pravachol Review and Pravachol Label ), ACYCLOVIR (200 Mg As Needed) (View Acyclovir Review and Acyclovir Label ). Patient was hospitalized.

6674533-1 | Gastritis, H1n1 Influenza, Transplant Rejection
Adverse event was reported on Mar 31, 2010 by a Female patient taking Myfortic (View Usage) (Dosage: 360 Mg, Daily) was diagnosed with blood pressure (What is blood pressure?), blood iron decreased, hypertension, oedema, immunosuppression, anaemia and. Location: UNITED STATES , child 9 years of age, Patient had the following side effects: gastritis, h1n1 influenza, transplant rejection. During the same period patient was treated with ENALAPRIL MALEATE (5 Mg Daily) (View Enalapril Maleate Review and Enalapril Maleate Label ), HECTOROL (2 Ug, Daily) (View Hectorol Review and Hectorol Label ), NIFEDIPINE (10 Mg As Needed) (View Nifedipine Review and Nifedipine Label ), NU IRON 150 (300 Mg, Daily) (View Nu-iron 150 Review and Nu-iron 150 Label ), LASIX (20 Mg, Daily) (View Lasix Review and Lasix Label ), PREDNISONE TAB (5 Mg, Daily) (View Prednisone Tab Review and Prednisone Tab Label ), EPOGEN (4000 U, Unk) (View Epogen Review and Epogen Label ), LIPITOR (20 Mg, Daily) (View Lipitor Review and Lipitor Label ). Patient was hospitalized.

6671842-7 | Pancytopenia
on Apr 01, 2010 Male patient from GERMANY , weighting 161.4 lb, was diagnosed with renal transplant and was treated with Myfortic (View Usage). After Myfortic was administered, patient had the following side effects: pancytopenia. Myfortic dosage: 1080 Mg, Bid. During the same period patient was treated with SANDIMMUNE (125 Mg 2 X 1) (View Sandimmune Review and Sandimmune Label ), SIMULECT (20 Mg) (View Simulect Review and Simulect Label ). Patient was hospitalized.

6671841-5 | Pancytopenia
on Apr 01, 2010 Male patient from GERMANY , weighting 161.4 lb, was diagnosed with renal transplant and was treated with Myfortic (View Usage). Patient experienced the following unwanted or unexpected effects: pancytopenia. Myfortic dosage: 1080 Mg, Bid. During the same period patient was treated with SANDIMMUNE (125 Mg 2 X 1) (View Sandimmune Review and Sandimmune Label ), SIMULECT (20 Mg) (View Simulect Review and Simulect Label ). Patient was hospitalized.

6663768-X | Condition Aggravated, Diarrhoea, Haemodialysis, Renal Failure Acute
Patient was taking Myfortic (View Usage). Patient had the following side effects: condition aggravated, diarrhoea, haemodialysis, renal failure acute on Mar 31, 2010 from UNITED STATES Additional patient health information: Female patient , 49 years of age, weighting 166.0 lb, was diagnosed with abdominal discomfort and. Myfortic dosage: 720 Mg Twice Daily Po. During the same period patient was treated with ATROVENT (View Atrovent Review and Atrovent Label ), ASPIRIN (View Aspirin Review and Aspirin Label ), ASOPT (View Asopt Review and Asopt Label ), AZITHROMYCIN (View Azithromycin Review and Azithromycin Label ), BENZONATATE (View Benzonatate Review and Benzonatate Label ), TESSALON (View Tessalon Review and Tessalon Label ), CALCIUM (View Calcium Review and Calcium Label ). Patient was hospitalized.