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Chantix Side Effects Report #5611346-3
Physician from FRANCE reported CHANTIX problem on Jan 21, 2008. Female patient, 55 years of age, was treated with CHANTIX. After drug was administered, patient experienced the following problems/side effects: bronchial hyperreactivity, bronchitis, . CHANTIX dosage: unknown. Patient recovered.

Chantix Side Effects Report #5628500-7
CHANTIX problem was reported by a Physician from FRANCE on Feb 07, 2008. Female patient, weighting 134.5 lb, was treated with CHANTIX. After drug was administered, patient experienced the following problems/side effects: bronchial hyperreactivity, bronchitis, . CHANTIX dosage: unknown. During the same period patient was treated with LEVOTHYROXINE. Patient recovered.

Vesicare Side Effects Report #5605816-1
Physician from JAPAN reported VESICARE problem on Jan 15, 2008. Male patient, 73 years of age, weighting 150.6 lb, was diagnosed with hypertonic bladder, bronchitis and was treated with VESICARE. After drug was administered, patient experienced the following problems/side effects: bronchial hyperreactivity, bronchitis, haemoptysis, lung disorder, malaise, po2 decreased, . VESICARE dosage: 5 MG, UID/QD, ORAL. During the same period patient was treated with DAZEN, PREDNISOLONE, BAKTAR, OMEPRAL, RABEPRAZOLE, MEDICON, MUCOSOLVAN, MUCODYNE. Patient was hospitalized. Patient recovered.

Herceptin Side Effects Report #5484370-1
HERCEPTIN problem was reported by a Consumer or non-health professional from UNITED KINGDOM on Sept 28, 2007. Female patient, weighting 105.8 lb, was diagnosed with breast cancer and was treated with HERCEPTIN. After drug was administered, patient experienced the following problems/side effects: bronchial hyperreactivity, . HERCEPTIN dosage: 160 MG, 1/WEEK. During the same period patient was treated with NAVELBINE, DOCETAXEL. Patient recovered.


Celebrex Side Effects Report #5460564-6
Consumer or non-health professional from UNITED STATES reported CELEBREX problem on Sept 10, 2007. Female patient, weighting 134.9 lb, was diagnosed with arthritis, pain and was treated with CELEBREX. After drug was administered, patient experienced the following problems/side effects: bronchial hyperreactivity, cardiac arrest, myocardial infarction, respiratory arrest, . CELEBREX dosage: TEXT:100MG AND 200MG-FREQ:INTERMITTENTLY ONCE OR TWICE DAILY. During the same period patient was treated with BEXTRA, VIOXX. Patient was hospitalized. Patient died on 02/14/2002.

Parlodel Side Effects Report #5413219-8
PARLODEL problem was reported by a Physician from UNITED STATES on Aug 03, 2007. Male patient, 59 years of age, was diagnosed with pituitary tumour benign and was treated with PARLODEL. After drug was administered, patient experienced the following problems/side effects: bronchial hyperreactivity, . PARLODEL dosage: unknown. Patient recovered.

Synagis Side Effects Report #5463889-3
Health Professional from UNITED STATES reported SYNAGIS problem on Mar 30, 2007. Female patient, weighting 17.20 lb, was treated with SYNAGIS. After drug was administered, patient experienced the following problems/side effects: bronchial hyperreactivity, ear infection, pyrexia, respiratory syncytial virus infection, upper respiratory tract infection, vomiting, . SYNAGIS dosage: unknown. Patient was hospitalized. Patient recovered.

Taxol Side Effects Report #5389211-9
TAXOL problem was reported by a Health Professional from SPAIN on July 16, 2007. Female patient, 47 years of age, was diagnosed with breast cancer, prophylaxis and was treated with TAXOL. After drug was administered, patient experienced the following problems/side effects: bronchial hyperreactivity, bronchospasm, emphysema, . TAXOL dosage: unknown. During the same period patient was treated with CYCLOPHOSPHAMIDE, MYOCET, OMEPRAZOLE, SINTROM. Patient was hospitalized. Patient recovered.

Taxol Side Effects Report #5389211-9
Health Professional from SPAIN reported TAXOL problem on July 16, 2007. Female patient, 47 years of age, was diagnosed with breast cancer, prophylaxis and was treated with TAXOL. After drug was administered, patient experienced the following problems/side effects: bronchial hyperreactivity, bronchospasm, emphysema, . TAXOL dosage: unknown. During the same period patient was treated with CYCLOPHOSPHAMIDE, MYOCET, OMEPRAZOLE, SINTROM. Patient was hospitalized. Patient recovered.


Paxil Side Effects Report #5780321-0
PAXIL problem was reported by a Consumer or non-health professional from UNITED STATES on June 12, 2008. Male patient was diagnosed with depression and was treated with PAXIL. After drug was administered, patient experienced the following problems/side effects: bronchial hyperreactivity, congenital anomaly, respiratory distress, . PAXIL dosage: 10MG PER DAY. During the same period patient was treated with PAROXETINE, VITAMIN. Patient was hospitalized. Patient recovered.

Paroxetine Side Effects Report #5734851-8
Consumer or non-health professional from UNITED STATES reported PAROXETINE problem on Apr 30, 2008. Male patient was diagnosed with depression and was treated with PAROXETINE. After drug was administered, patient experienced the following problems/side effects: bronchial hyperreactivity, congenital anomaly, . PAROXETINE dosage: 10MG PER DAY. During the same period patient was treated with VITAMIN. Patient was hospitalized. Patient recovered.

Opana Side Effects Report #5712268-X
OPANA ER problem was reported by a Physician from UNITED STATES on Apr 04, 2008. Male patient, 51 years of age, weighting 192.0 lb, was treated with OPANA ER. After drug was administered, patient experienced the following problems/side effects: bronchial hyperreactivity, wheezing, . OPANA ER dosage: unknown. Patient recovered.

Myozyme Side Effects Report #5361077-2
Physician from UNITED STATES reported MYOZYME problem on May 30, 2007. Male patient, weighting 13.01 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: bronchial hyperreactivity, candidiasis, central line infection, eosinophilia, haematuria, proteinuria, respiratory tract infection, staphylococcal infection, tachycardia, . MYOZYME dosage: 10 MG/KG Q2WKS IV. During the same period patient was treated with METHOTREXATE. Patient was hospitalized. Patient recovered.

Xolair Side Effects Report #5291082-6
XOLAIR problem was reported by a Consumer or non-health professional from GERMANY on Mar 26, 2007. Male patient, 14 years of age, was diagnosed with asthma and was treated with XOLAIR. After drug was administered, patient experienced the following problems/side effects: bronchial hyperreactivity, exercise tolerance decreased, . XOLAIR dosage: unknown. During the same period patient was treated with SULTANOL, SYMBICORT, PREDNISOLONE. Patient was hospitalized. Patient recovered.


Spiriva Side Effects Report #5293627-9
Physician from FRANCE reported SPIRIVA problem on Apr 03, 2007. Male patient, 73 years of age, was diagnosed with chronic obstructive pulmonary disease and was treated with SPIRIVA. After drug was administered, patient experienced the following problems/side effects: bronchial hyperreactivity, cough, . SPIRIVA dosage: unknown. Patient recovered.

Remicade Side Effects Report #5301596-8
REMICADE problem was reported by a Physician from UNITED STATES on Apr 10, 2007. Female patient, 44 years of age, was diagnosed with crohn's disease and was treated with REMICADE. After drug was administered, patient experienced the following problems/side effects: bronchial hyperreactivity, infusion related reaction, paraesthesia, . REMICADE dosage: unknown. During the same period patient was treated with PREDNISONE. Patient was hospitalized. Patient recovered.

Spiriva Side Effects Report #5308968-6
Physician from FRANCE reported SPIRIVA problem on Apr 19, 2007. Male patient, weighting 180.8 lb, was diagnosed with chronic obstructive pulmonary disease, increased bronchial secretion, arrhythmia, transient ischaemic attack, hypertension, cardiac failure, hiatus hernia and was treated with SPIRIVA. After drug was administered, patient experienced the following problems/side effects: bronchial hyperreactivity, cough, . SPIRIVA dosage: unknown. During the same period patient was treated with FLECAINIDE ACETATE, KARDEGIC, TEVETEN, LASIX, PARIET. Patient recovered.

Concerta Side Effects Report #5252223-X
CONCERTA problem was reported by a Physician from UNITED STATES on Feb 20, 2007. Male patient, weighting 67.99 lb, was treated with CONCERTA. After drug was administered, patient experienced the following problems/side effects: bronchial hyperreactivity, . CONCERTA dosage: unknown. Patient recovered.

Concerta Side Effects Report #5267048-9
Physician from UNITED STATES reported CONCERTA problem on Mar 07, 2007. Male patient, weighting 61.99 lb, was diagnosed with attention deficit/hyperactivity disorder and was treated with CONCERTA. After drug was administered, patient experienced the following problems/side effects: bronchial hyperreactivity, . CONCERTA dosage: unknown. Patient recovered.


Januvia Side Effects Report #5654543-3
JANUVIA problem was reported by a Physician from UNITED STATES on Dec 07, 2007. Female patient, 75 years of age, was diagnosed with type 2 diabetes mellitus and was treated with JANUVIA. After drug was administered, patient experienced the following problems/side effects: adverse event, bronchial hyperreactivity, . JANUVIA dosage: unknown. Patient was hospitalized. Patient recovered.

Vesicare Side Effects Report #5615130-6
Physician from JAPAN reported VESICARE problem on Jan 15, 2008. Male patient, 73 years of age, weighting 150.6 lb, was diagnosed with hypertonic bladder, bronchitis and was treated with VESICARE. After drug was administered, patient experienced the following problems/side effects: alveolitis allergic, bronchial hyperreactivity, bronchitis, cough, haemoptysis, lung disorder, malaise, po2 decreased, . VESICARE dosage: 5 MG, UID/QD, ORAL. During the same period patient was treated with DAZEN, PREDNISOLONE, BAKTAR, OMEPRAL PER ORAL NOS, PARIET, MEDICON, MUCOSOLVAN, MUCODYNE. Patient was hospitalized. Patient recovered.

Myozyme Side Effects Report #5566507-9
MYOZYME problem was reported by a Health Professional from UNITED STATES on Nov 30, 2007. Male patient, weighting 11.68 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: bacteria stool identified, bronchial hyperreactivity, central line infection, condition aggravated, enterobacter bacteraemia, eyelid function disorder, haemoglobin decreased, lobar pneumonia, nystagmus, . MYOZYME dosage: 20 MG/KG Q2WKS IV. During the same period patient was treated with BACTRIM, RITUXIMAB, METHOTREXATE, BENADRYL, TYLENOL. Patient was hospitalized. Patient recovered.

Myozyme Side Effects Report #5566517-1
Physician from UNITED STATES reported MYOZYME problem on Nov 30, 2007. Male patient, weighting 15.38 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: areflexia, bronchial hyperreactivity, candidiasis, central line infection, cleft lip, coagulopathy, condition aggravated, diaphragm muscle weakness, disease progression, . MYOZYME dosage: 30 MG/KG Q2WKS IV. During the same period patient was treated with METHOTREXATE, RITUXIMAB, IMMUNE GLOBULIN INTRAVENOUS. Patient was hospitalized. Patient recovered.

Vesicare Side Effects Report #5572491-4
VESICARE problem was reported by a Physician from JAPAN on Dec 05, 2007. Male patient, 73 years of age, weighting 150.6 lb, was diagnosed with hypertonic bladder, bronchitis and was treated with VESICARE. After drug was administered, patient experienced the following problems/side effects: alveolitis allergic, bronchial hyperreactivity, bronchitis, cough, haemoptysis, lung disorder, lymphocyte stimulation test positive, malaise, . VESICARE dosage: 5 MG, UID/QD, ORAL. During the same period patient was treated with DAZEN, PREDNISOLONE, BAKTAR, OMEPRAL PER ORAL NOS, PARIET, MEDICON, MUCOSOLVAN, MUCODYNE. Patient was hospitalized. Patient recovered.

Chantix Side Effects Report #5509470-9
Physician from UNITED STATES reported CHANTIX problem on Oct 26, 2007. Female patient, weighting 150.3 lb, was diagnosed with asthma, depression, hypersensitivity, myalgia, pain and was treated with CHANTIX. After drug was administered, patient experienced the following problems/side effects: basal cell carcinoma, bronchial hyperreactivity, chest discomfort, dyspnoea, heart rate decreased, insomnia, . CHANTIX dosage: unknown. During the same period patient was treated with ALBUTEROL, PROZAC, FLONASE, ACETYLSALICYLIC ACID SRT, ADVAIR DISKUS, ADVAIR DISKUS. Patient recovered.

Accutane Side Effects Report #5474949-5
ACCUTANE problem was reported by a Consumer or non-health professional from UNITED STATES on Sept 20, 2007. Male patient, 19 years of age, weighting 145.1 lb, was diagnosed with acne, bronchitis and was treated with ACCUTANE. After drug was administered, patient experienced the following problems/side effects: anaemia, bronchial hyperreactivity, chest pain, colitis, colitis ulcerative, deep vein thrombosis, depression, hyperthyroidism, ileal stenosis, . ACCUTANE dosage: DOSING REGIMEN 40 MG ON ODD DAYS AND 80 MG ON EVEN DAYS.. During the same period patient was treated with ZITHROMAX. Patient recovered.

Lamictal Side Effects Report #5482352-7
Consumer or non-health professional from UNITED STATES reported LAMICTAL problem on Oct 10, 2007. Male patient, 43 years of age, weighting 229.5 lb, was treated with LAMICTAL. After drug was administered, patient experienced the following problems/side effects: asthma, bronchial hyperreactivity, dyspnoea, . LAMICTAL dosage: 125MG TWICE PER DAY. During the same period patient was treated with RISPERDAL, CELEXA, BUPROPION, CLONAZEPAM, ASPIRIN, HYTRIN, LOPID, LOVASTAN. Patient recovered.

Accutane Side Effects Report #5483998-2
ACCUTANE problem was reported by a Consumer or non-health professional from UNITED STATES on Oct 02, 2007. Male patient, 19 years of age, weighting 145.1 lb, was diagnosed with acne, bronchitis and was treated with ACCUTANE. After drug was administered, patient experienced the following problems/side effects: anaemia, bronchial hyperreactivity, chest pain, colitis, colitis ulcerative, deep vein thrombosis, depression, hiatus hernia, hyperthyroidism, . ACCUTANE dosage: DOSING REGIMEN 40 MG ON ODD DAYS AND 80 MG ON EVEN DAYS.. During the same period patient was treated with ZITHROMAX. Patient was hospitalized. Patient recovered.

Accutane Side Effects Report #5484002-2
Physician from UNITED STATES reported ACCUTANE problem on Oct 03, 2007. Male patient, 23 years of age, weighting 145.9 lb, was diagnosed with acne, headache and was treated with ACCUTANE. After drug was administered, patient experienced the following problems/side effects: anaemia, bronchial hyperreactivity, colitis, colitis ulcerative, crohn's disease, depression, enteritis, enterocolitis infectious, gastrointestinal disorder, . ACCUTANE dosage: unknown. During the same period patient was treated with ADVIL LIQUI. Patient was hospitalized and became disabled. Patient recovered.

Lamictal Side Effects Report #5424955-1
LAMICTAL problem was reported by a Consumer or non-health professional from UNITED STATES on Aug 21, 2007. Male patient, 43 years of age, was treated with LAMICTAL. After drug was administered, patient experienced the following problems/side effects: asthma, bronchial hyperreactivity, dyspnoea, . LAMICTAL dosage: 125MG TWICE PER DAY. During the same period patient was treated with RISPERDAL, CELEXA, BUPROPION, CLONAZEPAM, ASPIRIN, HYTRIN, LOPID, LOVASTAN. Patient recovered.

Avandia Side Effects Report #5731864-7
Pharmacist from GERMANY reported AVANDIA problem on Apr 29, 2008. Male patient, 70 years of age, weighting 255.7 lb, was treated with AVANDIA. After drug was administered, patient experienced the following problems/side effects: asthma, bronchial hyperreactivity, cough, dyspnoea exertional, fluid retention, nocturia, obesity, oedema peripheral, productive cough, . AVANDIA dosage: 4MG PER DAY. During the same period patient was treated with MARCUMAR, BISOPROLOL, BISOPROLOL FUMARATE, AMLODIPINE, OLMESARTAN MEDOXOMIL, EBRANTIL, FLUVASTATIN, IBUPROFEN. Patient was hospitalized and became disabled. Patient recovered.

Velcade Side Effects Report #5747044-5
VELCADE problem was reported by a Physician from UNITED STATES on May 07, 2008. Male patient, 45 years of age, weighting 354.1 lb, was diagnosed with multiple myeloma and was treated with VELCADE. After drug was administered, patient experienced the following problems/side effects: bacterial infection, bronchial hyperreactivity, hypoxia, pneumonia, viral infection, . VELCADE dosage: 1 MG/M2. During the same period patient was treated with DEXAMETHASONE, THALIDOMIDE, CISPLATIN, DOXORUBICIN. Patient was hospitalized. Patient recovered.

Rimactane Side Effects Report #5716169-2
Physician from SWITZERLAND reported RIMACTANE problem on Apr 10, 2008. Female patient, 55 years of age, weighting 176.4 lb, was diagnosed with bladder cancer, urinary tract infection and was treated with RIMACTANE. After drug was administered, patient experienced the following problems/side effects: bovine tuberculosis, bronchial hyperreactivity, cholestasis, condition aggravated, cytolytic hepatitis, liver injury, lung neoplasm, sepsis, . RIMACTANE dosage: 600 MG, QD, ORAL. During the same period patient was treated with IMMUCYST, ROCEPHIN, RIMIFON, SIMCORA, PREDNISONE. Patient was hospitalized. Patient recovered.

Velcade Side Effects Report #5728179-X
VELCADE problem was reported by a Physician from UNITED STATES on Apr 21, 2008. Male patient, 45 years of age, weighting 354.1 lb, was diagnosed with multiple myeloma and was treated with VELCADE. After drug was administered, patient experienced the following problems/side effects: bacterial infection, bronchial hyperreactivity, pneumonia, viral infection, . VELCADE dosage: 1 MG/M2. During the same period patient was treated with DEXAMETHASONE, SYNTHROID, ACYCLOVIR, THALIDOMIDE, CISPLATIN, DOXORUBICIN. Patient was hospitalized. Patient recovered.

Myozyme Side Effects Report #5371492-9
Physician from UNITED STATES reported MYOZYME problem on June 08, 2007. Male patient, weighting 13.01 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: albuminuria, bronchial hyperreactivity, candidiasis, central line infection, eosinophilia, haematuria, influenza, proteinuria, pyrexia, . MYOZYME dosage: 10 MG/KG Q2WKS IV. During the same period patient was treated with METHOTREXATE. Patient was hospitalized. Patient recovered.

Accutane Side Effects Report #5374281-4
ACCUTANE problem was reported by a Consumer or non-health professional from UNITED STATES on May 08, 2007. Male patient, 23 years of age, weighting 145.9 lb, was diagnosed with acne, headache and was treated with ACCUTANE. After drug was administered, patient experienced the following problems/side effects: anaemia, bronchial hyperreactivity, colitis, colitis ulcerative, crohn's disease, depression, enteritis, enterocolitis infectious, gastrointestinal disorder, . ACCUTANE dosage: unknown. During the same period patient was treated with ADVIL LIQUI. Patient was hospitalized and became disabled. Patient recovered.

Accutane Side Effects Report #5329758-4
Consumer or non-health professional from UNITED STATES reported ACCUTANE problem on May 08, 2007. Male patient, 23 years of age, weighting 145.9 lb, was diagnosed with acne, headache and was treated with ACCUTANE. After drug was administered, patient experienced the following problems/side effects: anaemia, bronchial hyperreactivity, colitis, colitis ulcerative, crohn's disease, depression, enteritis, enterocolitis infectious, gastrointestinal disorder, . ACCUTANE dosage: unknown. During the same period patient was treated with ADVIL. Patient was hospitalized and became disabled. Patient recovered.

Myozyme Side Effects Report #5339706-9
MYOZYME problem was reported by a Physician from UNITED STATES on May 11, 2007. Male patient was diagnosed with glycogen storage disease type ii and was treated with MYOZYME. After drug was administered, patient experienced the following problems/side effects: blood urine, bronchial hyperreactivity, candidiasis, central line infection, eosinophilia, haematuria, influenza, infusion related reaction, protein urine present, . MYOZYME dosage: 20 MG/KG Q2WKS IV. During the same period patient was treated with METHOTREXATE. Patient was hospitalized. Patient recovered.

Paxil Side Effects Report #5675882-6
Health Professional from UNITED STATES reported PAXIL problem on Mar 07, 2008. Male patient, weighting 4.85 lb, was diagnosed with panic attack, anxiety, constipation and was treated with PAXIL. After drug was administered, patient experienced the following problems/side effects: acidosis, atrial septal defect, bronchial hyperreactivity, cardiac disorder, cardiac failure congestive, cerebral haemorrhage, cholestasis, congenital anomaly, congenital pulmonary hypertension, . PAXIL dosage: 20MG PER DAY. During the same period patient was treated with PAROXETINE, VITAMIN CAP, FERROUS SULPHATE, CHLOROTHIAZIDE, DIGOXIN, PHENOBARBITAL, POLYVISOL, COLACE. Patient was hospitalized. Patient recovered.

Accutane Side Effects Report #5612014-4
ACCUTANE problem was reported by a Physician from UNITED STATES on Jan 21, 2008. Male patient, 23 years of age, weighting 145.9 lb, was diagnosed with acne, headache and was treated with ACCUTANE. After drug was administered, patient experienced the following problems/side effects: anaemia, anal fistula, bronchial hyperreactivity, colitis, colitis ulcerative, crohn's disease, depression, enteritis, enterocolitis infectious, . ACCUTANE dosage: unknown. During the same period patient was treated with ADVIL LIQUI. Patient was hospitalized and became disabled. Patient recovered.

Xopenex Side Effects Report #5621846-8
Consumer or non-health professional from UNITED STATES reported XOPENEX problem on Jan 23, 2008. Male patient, child 1. years of age, was diagnosed with wheezing and was treated with XOPENEX. After drug was administered, patient experienced the following problems/side effects: apnoea, arthropod bite, bronchial hyperreactivity, complex partial seizures, cough, staring, sydenham's chorea, tardive dyskinesia, treatment noncompliance, . XOPENEX dosage: 1.25 MG/3ML; PRN; INHALATION. During the same period patient was treated with PULMICORT, ROBITUSSIN, ALBUTEROL. Patient recovered.

Accutane Side Effects Report #5644389-4
ACCUTANE problem was reported by a Physician from UNITED STATES on Feb 20, 2008. Male patient, 23 years of age, weighting 145.9 lb, was diagnosed with acne, headache and was treated with ACCUTANE. After drug was administered, patient experienced the following problems/side effects: anaemia, anal fistula, bronchial hyperreactivity, colitis, colitis ulcerative, crohn's disease, depression, enteritis, enterocolitis infectious, . ACCUTANE dosage: unknown. During the same period patient was treated with ADVIL. Patient was hospitalized and became disabled. Patient recovered.

Risperdal Side Effects Report #5585217-5
Consumer or non-health professional from UNITED STATES reported RISPERDAL problem on Jan 02, 2008. Female patient, weighting 220.0 lb, was diagnosed with mania and was treated with RISPERDAL. After drug was administered, patient experienced the following problems/side effects: angiopathy, blood calcium increased, bronchial hyperreactivity, diabetes mellitus, myocardial infarction, pneumonia, pulmonary oedema, tachycardia, tremor, . RISPERDAL dosage: unknown. During the same period patient was treated with SEROQUEL, ZYPREXA, VITAMIN E, ASCORBIC ACID, WELLBUTRIN, DEPAKOTE, ESTROGEN. Patient recovered.

Myozyme Side Effects Report #5384925-9
MYOZYME problem was reported by a Physician from UNITED STATES on June 25, 2007. Male patient, weighting 13.01 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: alanine aminotransferase increased, aspartate aminotransferase increased, bronchial hyperreactivity, candidiasis, central line infection, eosinophilia, hypotension, influenza, renal failure acute, . MYOZYME dosage: 10 MG/KG Q2WKS IV. During the same period patient was treated with DIGOXIN, POTASSIUM CHLORIDE, CALCIUM GLUBIONATE, PROCRIT, BENADRYL, TYLENOL, FERROUS SULPHATE. Patient was hospitalized. Patient recovered.

Myozyme Side Effects Report #5394686-5
Physician from UNITED STATES reported MYOZYME problem on July 09, 2007. Male patient, weighting 13.01 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: alanine aminotransferase increased, aspartate aminotransferase increased, bronchial hyperreactivity, candidiasis, central line infection, enzyme inhibition, eosinophilia, hypotension, influenza serology positive, . MYOZYME dosage: 10 MG/KG QWKS IV. During the same period patient was treated with METHOTREXATE, CAPTOPRIL, FUROSEMIDE, DIGOXIN, POTASSIUM CHLORIDE, CALCIUM GLUBIONATE, PROCRIT. Patient was hospitalized. Patient recovered.

Myozyme Side Effects Report #5384925-9
MYOZYME problem was reported by a Physician from UNITED STATES on June 25, 2007. Male patient, weighting 13.01 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: alanine aminotransferase increased, aspartate aminotransferase increased, bronchial hyperreactivity, candidiasis, central line infection, eosinophilia, hypotension, influenza, renal failure acute, . MYOZYME dosage: 10 MG/KG Q2WKS IV. During the same period patient was treated with DIGOXIN, POTASSIUM CHLORIDE, CALCIUM GLUBIONATE, PROCRIT, BENADRYL, TYLENOL, FERROUS SULPHATE. Patient was hospitalized. Patient recovered.

Myozyme Side Effects Report #5394686-5
Physician from UNITED STATES reported MYOZYME problem on July 09, 2007. Male patient, weighting 13.01 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: alanine aminotransferase increased, aspartate aminotransferase increased, bronchial hyperreactivity, candidiasis, central line infection, enzyme inhibition, eosinophilia, hypotension, influenza serology positive, . MYOZYME dosage: 10 MG/KG QWKS IV. During the same period patient was treated with METHOTREXATE, CAPTOPRIL, FUROSEMIDE, DIGOXIN, POTASSIUM CHLORIDE, CALCIUM GLUBIONATE, PROCRIT. Patient was hospitalized. Patient recovered.

Ventavis Side Effects Report #5748305-6
VENTAVIS problem was reported by a Physician from UNITED STATES on May 06, 2008. Male patient, child 12 years of age, weighting 92.59 lb, was diagnosed with pulmonary arterial hypertension and was treated with VENTAVIS. After drug was administered, patient experienced the following problems/side effects: abdominal pain upper, arthropod bite, bronchial hyperreactivity, bronchospasm, eye disorder, movement disorder, nausea, obstructive airways disorder, oral disorder, . VENTAVIS dosage: unknown. During the same period patient was treated with TRACLEER, REVATIO, ZYRTEC, REMODULIN. Patient recovered.

Paxil Side Effects Report #5690759-8
Health Professional from UNITED STATES reported PAXIL problem on Mar 19, 2008. Male patient, weighting 4.85 lb, was diagnosed with panic attack, anxiety, constipation and was treated with PAXIL. After drug was administered, patient experienced the following problems/side effects: acidosis, atrial septal defect, bronchial hyperreactivity, cardiac disorder, cardiac failure congestive, cerebral haemorrhage, cholestasis, congenital anomaly, congenital pulmonary hypertension, . PAXIL dosage: 20MG PER DAY. During the same period patient was treated with PAROXETINE, VITAMIN CAP, FERROUS SULPHATE, CHLOROTHIAZIDE, DIGOXIN, PHENOBARBITAL, POLYVISOL, COLACE. Patient was hospitalized. Patient recovered.

Myozyme Side Effects Report #5706625-5
MYOZYME problem was reported by a Health Professional from UNITED STATES on Apr 02, 2008. Male patient, weighting 11.68 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: bacteraemia, bacteria stool identified, bronchial hyperreactivity, catheter related infection, central line infection, clostridial infection, enterobacter infection, eyelid disorder, lobar pneumonia, . MYOZYME dosage: 20 MG/KG, Q2W, INTRAVENOUS. During the same period patient was treated with BACTRIM, RITUXIMAB, METHOTREXATE, BENADRYL, ACETAMINOPHEN. Patient was hospitalized. Patient recovered.

Myozyme Side Effects Report #5372572-4
Physician from MALAYSIA reported MYOZYME problem on June 12, 2007. Female patient, weighting 13.23 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: arrhythmia, asthma, bronchial hyperreactivity, bronchospasm, pneumonia aspiration, ventricular fibrillation, . MYOZYME dosage: 20 MG/KG Q2WKS IV. Patient died on 06/12/2007.