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Mycophenolate Side Effects Report #5403912-5
Physician from UNITED STATES reported MYCOPHENOLATE MOFETI problem on Oct 24, 2006. Male patient, 16 years of age, was diagnosed with prophylaxis against transplant rejection and was treated with MYCOPHENOLATE MOFETI. After drug was administered, patient experienced the following problems/side effects: haemophilus infection, mycobacterial infection, . MYCOPHENOLATE MOFETI dosage: unknown. During the same period patient was treated with TACROLIMUS, PREDNISONE. Patient recovered.

Mycophenolate Side Effects Report #5403912-5
MYCOPHENOLATE MOFETI problem was reported by a Physician from UNITED STATES on Oct 24, 2006. Male patient, 16 years of age, was diagnosed with prophylaxis against transplant rejection and was treated with MYCOPHENOLATE MOFETI. After drug was administered, patient experienced the following problems/side effects: haemophilus infection, mycobacterial infection, . MYCOPHENOLATE MOFETI dosage: unknown. During the same period patient was treated with TACROLIMUS, PREDNISONE. Patient recovered.

Humira Side Effects Report #5768454-6
Consumer or non-health professional from UNITED STATES reported HUMIRA problem on Mar 05, 2008. Male patient, weighting 245.2 lb, was diagnosed with psoriatic arthropathy, psoriasis and was treated with HUMIRA. After drug was administered, patient experienced the following problems/side effects: haemophilus infection, . HUMIRA dosage: unknown. Patient recovered.

Velcade Side Effects Report #5754022-9
VELCADE problem was reported by a Physician from FRANCE on May 12, 2008. Male patient, 59 years of age, was diagnosed with multiple myeloma and was treated with VELCADE. After drug was administered, patient experienced the following problems/side effects: haemophilus infection, syncope vasovagal, . VELCADE dosage: 2.60 MG. During the same period patient was treated with DEXAMETHASONE. Patient was hospitalized. Patient recovered.


Prograf Side Effects Report #5679810-9
Health Professional from AUSTRIA reported PROGRAF problem on Nov 16, 2007. Male patient, 45 years of age, was diagnosed with renal transplant and was treated with PROGRAF. After drug was administered, patient experienced the following problems/side effects: bronchitis, haemophilus infection, hla marker study, nephrosclerosis, pneumonia, proteinuria, rash, varicella, . PROGRAF dosage: unknown. During the same period patient was treated with MYCOPHENOLATE MOFETIL. Patient recovered.

Temodal Side Effects Report #5591120-7
TEMODAL problem was reported by a Physician from JAPAN on Jan 07, 2008. Male patient, 66 years of age, weighting 110.2 lb, was diagnosed with glioblastoma multiforme and was treated with TEMODAL. After drug was administered, patient experienced the following problems/side effects: c-reactive protein increased, haemophilus infection, inflammation, neutrophil count increased, pneumonia, pneumonia primary atypical, sputum culture positive, . TEMODAL dosage: unknown. During the same period patient was treated with ZOFRAN ZYDIS, ZONISAMIDE, GLYSENNID. Patient was hospitalized. Patient recovered.

Synagis Side Effects Report #5602412-7
Physician from UNITED STATES reported SYNAGIS problem on Jan 10, 2008. Female patient was diagnosed with de lange's syndrome, foetal growth retardation, premature baby and was treated with SYNAGIS. After drug was administered, patient experienced the following problems/side effects: feeding disorder, haemophilus infection, lethargy, moraxella infection, pallor, pneumonia respiratory syncytial viral, respiratory failure, upper respiratory tract infection, . SYNAGIS dosage: 55 MG, 1 IN 1 M, INTRAMUSCULAR; 50 MG, 1 IN 1 M, INTRAMUSCULAR; 50 MG, 1 IN 1 M, INTRAMUSCULAR. Patient was hospitalized. Patient recovered.

Carbamazepine Side Effects Report #5489127-3
CARBAMAZEPINE problem was reported by a Consumer or non-health professional from BULGARIA on Oct 08, 2007. Male patient, 28 years of age, was treated with CARBAMAZEPINE. After drug was administered, patient experienced the following problems/side effects: haemophilus infection, hepatosplenomegaly, pneumonia, sputum culture positive, toxic epidermal necrolysis, . CARBAMAZEPINE dosage: 600 MG QD. During the same period patient was treated with CLONIDINE, DIAZEPAM, ALCOHOL. Patient was hospitalized. Patient recovered.

Amoxicillin Side Effects Report #5406907-0
Consumer or non-health professional from NETHERLANDS reported AMOXICILLIN TRIHYDRATE problem on July 20, 2007. Male patient, 70 years of age, was treated with AMOXICILLIN TRIHYDRATE. After drug was administered, patient experienced the following problems/side effects: conjunctivitis, haemophilus infection, ileus, staphylococcal infection, stomatitis, toxic epidermal necrolysis, . AMOXICILLIN TRIHYDRATE dosage: unknown. Patient was hospitalized. Patient recovered.


Tysabri Side Effects Report #5778163-5
TYSABRI problem was reported by a Physician from UNITED STATES on June 03, 2008. Female patient was diagnosed with multiple sclerosis and was treated with TYSABRI. After drug was administered, patient experienced the following problems/side effects: convulsion, haemophilus infection, opportunistic infection, sinusitis, . TYSABRI dosage: 300 MG;QM;IV. Patient was hospitalized. Patient recovered.

Mirena Side Effects Report #5360845-0
Physician from UNITED STATES reported MIRENA problem on June 12, 2007. Female patient was treated with MIRENA. After drug was administered, patient experienced the following problems/side effects: abdominal pain, haemophilus infection, headache, iucd complication, vomiting, . MIRENA dosage: unknown. Patient was hospitalized. Patient recovered.

Myozyme Side Effects Report #5330603-1
MYOZYME problem was reported by a Physician from TAIWAN, PROVINCE OF CHINA on May 05, 2007. Male patient, child 4 years of age, weighting 37.92 lb, was diagnosed with glycogen storage disease type ii and was treated with MYOZYME. After drug was administered, patient experienced the following problems/side effects: bacterial infection, haemophilus infection, pneumonia, serratia infection, skin lesion, streptococcal infection, type iii immune complex mediated reaction, . MYOZYME dosage: 10 MG/KG Q2WKS IV. During the same period patient was treated with ALPHA, CARDILOL. Patient was hospitalized. Patient recovered.

Synagis Side Effects Report #5306562-4
Physician from FRANCE reported SYNAGIS problem on Apr 03, 2007. Female patient, weighting 7.32 lb, was diagnosed with antiviral prophylaxis, premature baby and was treated with SYNAGIS. After drug was administered, patient experienced the following problems/side effects: bronchiolitis, haemophilus infection, viral rhinitis, . SYNAGIS dosage: 50 MG, 1 IN 30 D, INTRAMUSCULAR. During the same period patient was treated with VITAMIN D, FLUOR. Patient was hospitalized. Patient recovered.

Synagis Side Effects Report #5313606-2
SYNAGIS problem was reported by a Physician from FRANCE on Apr 10, 2007. Female patient, weighting 6.06 lb, was diagnosed with antiviral prophylaxis and was treated with SYNAGIS. After drug was administered, patient experienced the following problems/side effects: asthma, haemophilus infection, lung disorder, . SYNAGIS dosage: unknown. Patient was hospitalized. Patient recovered.


Tiotropium Side Effects Report #5599074-4
Consumer or non-health professional from reported TIOTROPIUM problem on Jan 16, 2008. Male patient, 65 years of age, was diagnosed with chronic obstructive pulmonary disease and was treated with TIOTROPIUM. After drug was administered, patient experienced the following problems/side effects: alpha haemolytic streptococcal infection, chronic obstructive pulmonary disease, haemophilus infection, neisseria infection, pseudomonas infection, . TIOTROPIUM dosage: unknown. Patient was hospitalized. Patient recovered.

Leflunomide Side Effects Report #5552647-7
LEFLUNOMIDE problem was reported by a Consumer or non-health professional from NETHERLANDS on Nov 29, 2007. Female patient, 60 years of age, was diagnosed with psoriatic arthropathy and was treated with LEFLUNOMIDE. After drug was administered, patient experienced the following problems/side effects: anaemia, enterobacter infection, haemophilus infection, pneumonia, pseudomonas infection, pulmonary cavitation, staphylococcal infection, . LEFLUNOMIDE dosage: 20 MG. During the same period patient was treated with METHOTREXATE, PREDNISONE, HYDROXYCHLOROQUINE, SULPHASALAZINE. Patient recovered.

Tiotropium Side Effects Report #5512071-X
Consumer or non-health professional from reported TIOTROPIUM problem on Nov 05, 2007. Male patient, 65 years of age, was diagnosed with chronic obstructive pulmonary disease and was treated with TIOTROPIUM. After drug was administered, patient experienced the following problems/side effects: alpha haemolytic streptococcal infection, chronic obstructive pulmonary disease, haemophilus infection, neisseria infection, pseudomonas infection, . TIOTROPIUM dosage: unknown. Patient was hospitalized. Patient recovered.

Synagis Side Effects Report #5378448-0
SYNAGIS problem was reported by a Physician from FRANCE on June 20, 2007. Female patient was diagnosed with antiviral prophylaxis and was treated with SYNAGIS. After drug was administered, patient experienced the following problems/side effects: anorexia, gastroenteritis, haemophilus infection, increased bronchial secretion, respiratory tract infection, tracheomalacia, . SYNAGIS dosage: unknown. Patient was hospitalized. Patient recovered.

Synagis Side Effects Report #5378448-0
Physician from FRANCE reported SYNAGIS problem on June 20, 2007. Female patient was diagnosed with antiviral prophylaxis and was treated with SYNAGIS. After drug was administered, patient experienced the following problems/side effects: anorexia, gastroenteritis, haemophilus infection, increased bronchial secretion, respiratory tract infection, tracheomalacia, . SYNAGIS dosage: unknown. Patient was hospitalized. Patient recovered.


Mycophenolic Side Effects Report #5771432-4
MYCOPHENOLIC ACID ERL problem was reported by a Physician from BELGIUM on June 06, 2008. Female patient, weighting 160.9 lb, was diagnosed with renal transplant and was treated with MYCOPHENOLIC ACID ERL. After drug was administered, patient experienced the following problems/side effects: c-reactive protein increased, dyspnoea, haemophilus infection, oral candidiasis, pharyngitis, pneumonia pneumococcal, productive cough, respiratory distress, . MYCOPHENOLIC ACID ERL dosage: 1440MG DAY. During the same period patient was treated with MYCOPHENOLIC ACID ERL, NEORAL. Patient was hospitalized. Patient recovered.

Mycophenolic Side Effects Report #5754049-7
Physician from BELGIUM reported MYCOPHENOLIC ACID ERL problem on May 21, 2008. Female patient, weighting 160.9 lb, was diagnosed with renal transplant and was treated with MYCOPHENOLIC ACID ERL. After drug was administered, patient experienced the following problems/side effects: c-reactive protein increased, dyspnoea, haemophilus infection, oral candidiasis, pharyngitis, pneumonia pneumococcal, productive cough, respiratory distress, . MYCOPHENOLIC ACID ERL dosage: 1440MG DAY. During the same period patient was treated with MYCOPHENOLIC ACID ERL, NEORAL. Patient was hospitalized. Patient recovered.

Clarithromycin Side Effects Report #5357254-7
CLARITHROMYCIN problem was reported by a Physician from ITALY on June 01, 2007. Female patient, 54 years of age, was diagnosed with haemophilus infection and was treated with CLARITHROMYCIN. After drug was administered, patient experienced the following problems/side effects: haemophilus infection, nephropathy toxic, renal impairment, . CLARITHROMYCIN dosage: unknown. During the same period patient was treated with SIROLIMUS, PREDNISONE, OMEPRAZOLE, GLYCERYL TRINITRATE, CEFTAZIDIME, ALLOPURINOL, ASPIRIN, DARBEPOETIN ALFA. Patient was hospitalized. Patient recovered.

Synagis Side Effects Report #5273509-9
Physician from FRANCE reported SYNAGIS problem on Mar 06, 2007. Male patient, weighting 7.52 lb, was diagnosed with antiviral prophylaxis and was treated with SYNAGIS. After drug was administered, patient experienced the following problems/side effects: acute respiratory failure, bronchiolitis, haemophilus infection, respiratory syncytial virus infection, . SYNAGIS dosage: 48 MG, 1 IN 30 D, INTRAMUSCULAR. During the same period patient was treated with SPIRONOLACTONE. Patient was hospitalized. Patient recovered.