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Idursulfase adverse events reported to FDA.

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Summary

FDA Adverse Reports: 6. View All

Idursulfase FDA safety alerts: No

Reported deaths: 6

Reported hospitalizations: 6

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Often additional risks of using a medication, such as Idursulfase, become known after product is used by a larger number of patients, for a longer period of time, and by patients with different health characteristics from those studied before drug approval. This page allows You to Find answers and discuss health symptoms with other Idursulfase users, Learn more about unwanted side effects & find ways to reduce them. Browse Idursulfase Adverse Reports reported to FDA and participate in Idursulfase discussion, find alternative treatments and find ways to avoid or reduce risks associated with using Idursulfase. You can also Post a question to users community or Ask a Doctor. PatientsVille.com is Your Complete Guide to all common, undocumented and undisclosed side effects associated with drugs and vaccines. Browse More Drug Reports Here: A  B  C  D  E  F  G  H  I  J  K  L  M  N  O  P  Q  R  S  T  U  V  W  X  Y  Z

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Idursulfase Adverse Effect Reports (FDA)

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7022468-7 | Idiopathic Thrombocytopenic Purpura
on Sep 24, 2010 Male patient from TURKEY , 20 years of age, was diagnosed with mucopolysaccharidosis ii and was treated with Idursulfase (View Usage). Patient experienced the following unwanted or unexpected effects: idiopathic thrombocytopenic purpura. Idursulfase dosage: .5 Mg/kg, 1x/week.

6899457-6 | Eyelid Oedema, Infusion Related Reaction, Respiratory Disorder, Urticaria
Patient was taking Idursulfase (View Usage). Patient had the following side effects: eyelid oedema, infusion related reaction, respiratory disorder, urticaria on Jul 29, 2010 from JAPAN Additional patient health information: Male patient , weighting 61.73 lb, was diagnosed with mucopolysaccharidosis ii and. Idursulfase dosage: . During the same period patient was treated with LORATADINE (10 Mg, 1x/day:qd) (View Loratadine Review and Loratadine Label ), HYDROXYZINE PAMOATE (25 Mg, One Dose) (View Hydroxyzine Pamoate Review and Hydroxyzine Pamoate Label ), METHYLPREDNISOLONE SODIUM SUCCINATE (20 Mg, One Dose) (View Methylprednisolone Sodium Succinate Review and Methylprednisolone Sodium Succinate Label ), HYDROCORTISONE SODIUM SUCCINATE (300 Mg, One Dose) (View Hydrocortisone Sodium Succinate Review and Hydrocortisone Sodium Succinate Label ).

6818969-4 | Epilepsy
Adverse event was reported on Jun 25, 2010 by a Male patient taking Idursulfase (View Usage) (Dosage: 11.2 Mg, 1x/week) was diagnosed with mucopolysaccharidosis ii and. Location: UNITED STATES , weighting 50.71 lb, After Idursulfase was administered, patient had the following side effects: epilepsy (What is epilepsy?). During the same period patient was treated with CHLORPHENIRAMINE MALEATE (.5 Ml, Unk) (View Chlorpheniramine Maleate Review and Chlorpheniramine Maleate Label ).

6743366-X | Infusion Related Reaction, Respiratory Distress
on May 20, 2010 Male patient from BRAZIL , weighting 33.07 lb, was diagnosed with mucopolysaccharidosis ii, upper respiratory tract infection and was treated with Idursulfase (View Usage). Patient experienced the following unwanted or unexpected effects: infusion related reaction, respiratory distress. Idursulfase dosage: Unk, 1x/week. During the same period patient was treated with PENICILLIN /00000901/ (Unk, Unk) (View Penicillin /00000901/ Review and Penicillin /00000901/ Label ).


5406182-7 | Blood Immunoglobulin G Increased, Blood Potassium Decreased, Blood Sodium Decreased, Decreased Appetite, Diarrhoea, Dysgeusia, Fatigue, Iron Deficiency Anaemia, Pharyngitis Streptococcal
on Jul 18, 2007 Male patient from UNITED STATES , child 8 years of age, weighting 50.04 lb, was diagnosed with mucopolysaccharidosis ii and was treated with Idursulfase (View Usage). Patient had the following side effects: blood immunoglobulin g increased, blood potassium decreased, blood sodium decreased, decreased appetite, diarrhoea, dysgeusia, fatigue, iron deficiency anaemia, pharyngitis streptococcal. Idursulfase dosage: (11.5 Mg, 1 In 1 Wk), Intravenous Drip. During the same period patient was treated with NASONEX (View Nasonex Review and Nasonex Label ), SINGULAIR (View Singulair Review and Singulair Label ). Patient was hospitalized.

5371757-0 | Appendicitis, Peritonitis
Patient was taking Idursulfase (View Usage). After Idursulfase was administered, patient had the following side effects: appendicitis (What is appendicitis?), peritonitis on Jun 07, 2007 from SPAIN Additional patient health information: Male patient , 18 years of age, weighting 92.59 lb, was diagnosed with mucopolysaccharidosis ii and. Idursulfase dosage: 21 Mg, 1 In 1 Wk, Intraveous Drip. During the same period patient was treated with ENALAPRIL (ENALAPRIL ) (View Enalapril (enalapril ) Review and Enalapril (enalapril ) Label ). Patient was hospitalized.


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To find out about documented side effects or safety concerns read either the drug label or the drug's package insert. You may also want to speak with your pharmacist or healthcare provider. All medicines have benefits and risks. The risks are the chances that something unwanted or unexpected could happen to you when you use them. You can protect yourself by searching summaries of recent safety alerts, adverse reports. Sometimes there are risks that only come to light after a medical product gets on the market and is used in a larger number of patients, for a longer period of time, and in patients whose health characteristics are different from those of the patients studied before approval.

Be aware of the following potential Idursulfase risks to be aware of: 1. Watch for any Serious adverse events, such as life-threatening situation, which can require an admission to hospital or longer-than-expected hospital stay, permanent disability, birth defect, miscarriage, stillbirth, or birth with serious disease requires medical care to prevent permanent damage
2. Any potential Idursulfase quality problem: suspected counterfeit product, potentially contaminated product indicated by suspicious odor or unusual color, inaccurate or unreadable product labeling
3. Potential Idursulfase use error: mixing up products with similar drug names or packaging, taking wrong dose of a drug because of confusing dosing instructions on label
4. When applicable, Problems with different manufacturer of same medicine: not getting same results from a generic drug as a brand name drug, or from another generic

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Idursulfase Reactions
AppendicitisWhat is Appendicitis?
Blood Immunoglobulin G Increased
Blood Potassium Decreased
Blood Sodium Decreased
Decreased Appetite
Diarrhoea
Dysgeusia
EpilepsyWhat is Epilepsy?
Eyelid Oedema
Fatigue
Idiopathic Thrombocytopenic Purpura
Infusion Related Reaction
Iron Deficiency Anaemia
Peritonitis
Pharyngitis Streptococcal
Respiratory Disorder
Respiratory Distress
Urticaria
Idursulfase Side Effects Notice - The material on this site is for informational purposes only, and is not a substitute for medical advice, diagnosis or treatment provided by a qualified health care provider. PatientsVille.com does not provide medical advice, diagnosis or treatment. The information regarding Idursulfase adverse reports, reviews and polls contained on PatientsVille.com site has not been scientifically or otherwise verified as to a cause and effect relationship and cannot be used to estimate the incidence of adverse drug reactions or for establishing or changing of patient treatments. Thank you for visiting Patientsville.com!