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Deferoxamine adverse events reported to FDA.

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Summary

FDA Adverse Reports: 6. View All

Deferoxamine FDA safety alerts: No

Reported deaths: 10

Reported hospitalizations: 7

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Often additional risks of using a medication, such as Deferoxamine, 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 Deferoxamine users, Learn more about unwanted side effects & find ways to reduce them. Browse Deferoxamine Adverse Reports reported to FDA and participate in Deferoxamine discussion, find alternative treatments and find ways to avoid or reduce risks associated with using Deferoxamine. 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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Deferoxamine Adverse Effect Reports (FDA)

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4778678-2 | Caesarean Section, Congestive Cardiomyopathy, Dilatation Ventricular, Dyspnoea, Ejection Fraction Decreased, Electrocardiogram T Wave Inversion, Fatigue, Gallop Rhythm Present
on Jun 15, 2005 Female patient from GREECE , 28 years of age, was diagnosed with congestive cardiomyopathy and was treated with Deferoxamine (View Usage). Patient experienced the following unwanted or unexpected effects: caesarean section, congestive cardiomyopathy, dilatation ventricular, dyspnoea, ejection fraction decreased, electrocardiogram t wave inversion, fatigue, gallop rhythm present. Deferoxamine dosage: 50 Mg/kg 5 Days/week. During the same period patient was treated with DIGOXIN (0.125 Mg 5 Days/week) (View Digoxin Review and Digoxin Label ).

4778669-1 | Cardiac Arrest
Patient was taking Deferoxamine (View Usage). Patient had the following side effects: cardiac arrest (What is cardiac arrest?) on Aug 24, 2005 from UNITED STATES Additional patient health information: Male patient , child 5 years of age, was diagnosed with autism (What is autism?) and. Deferoxamine dosage: 3 Times.

4738251-9 | Leukocytoclastic Vasculitis, Pruritus, Urticaria
Adverse event was reported on Apr 05, 2005 by a Male patient taking Deferoxamine (View Usage) (Dosage: 2 G, Once/single) was diagnosed with blood iron increased, whole blood transfusion and. Location: UNITED STATES , 32 years of age, weighting 108.0 lb, After Deferoxamine was administered, patient had the following side effects: leukocytoclastic vasculitis, pruritus, urticaria. During the same period patient was treated with DIPHENHYDRAMINE HCL (25 Mg, Qd) (View Diphenhydramine Hcl Review and Diphenhydramine Hcl Label ), ACETAMINOPHEN (650 Mg, Qd) (View Acetaminophen Review and Acetaminophen Label ), FOLIC ACID (1 Mg, Qd) (View Folic Acid Review and Folic Acid Label ), CALCIUM CARBONATE (1.5 G, Qd) (View Calcium Carbonate Review and Calcium Carbonate Label ).

4700171-3 | Caesarean Section, Congestive Cardiomyopathy, Dilatation Ventricular, Dyspnoea, Ejection Fraction Decreased, Electrocardiogram T Wave Inversion, Fatigue, Gallop Rhythm Present
on Jun 15, 2005 Female patient from , 28 years of age, was diagnosed with congestive cardiomyopathy and was treated with Deferoxamine (View Usage). Patient experienced the following unwanted or unexpected effects: caesarean section, congestive cardiomyopathy, dilatation ventricular, dyspnoea, ejection fraction decreased, electrocardiogram t wave inversion, fatigue, gallop rhythm present. Deferoxamine dosage: 50 Mg/kg 5 Days/week. During the same period patient was treated with DIGOXIN (0.125 Mg 5 Days/week) (View Digoxin Review and Digoxin Label ).


4560187-7 | Colour Vision Tests Abnormal, Deafness, Dental Caries, Dry Mouth, Keratoconjunctivitis Sicca, Punctate Keratitis, Retinal Pigment Epitheliopathy, Sjogren's Syndrome
on Dec 06, 2004 Female patient from , 64 years of age, was diagnosed with blood iron increased and was treated with Deferoxamine (View Usage). Patient had the following side effects: colour vision tests abnormal, deafness, dental caries, dry mouth, keratoconjunctivitis sicca, punctate keratitis, retinal pigment epitheliopathy, sjogren's syndrome (What is sjogren's syndrome?). Deferoxamine dosage: 6 Days Per Week.

4554329-7 | Blood Pressure Decreased, Cardiovascular Disorder, Feeling Abnormal, Loss Of Consciousness, Pyrexia, Syncope
Patient was taking Deferoxamine (View Usage). After Deferoxamine was administered, patient had the following side effects: blood pressure decreased, cardiovascular disorder, feeling abnormal, loss of consciousness, pyrexia, syncope on Jan 05, 2005 from Additional patient health information: Male patient , 82 years of age, was diagnosed with blood iron increased and. Deferoxamine dosage: . 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 Deferoxamine 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 Deferoxamine quality problem: suspected counterfeit product, potentially contaminated product indicated by suspicious odor or unusual color, inaccurate or unreadable product labeling
3. Potential Deferoxamine 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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Folate dosage: . During the same period patient was treated with DEFEROXAMINE MESYLATE, BLOOD TRANSFUSION, OXYMETHOLONE, PREDNISONE. Patient died.

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Deferoxamine Reactions
Blood Pressure Decreased
Caesarean Section
Cardiac ArrestWhat is Cardiac arrest?
Cardiovascular Disorder
Colour Vision Tests Abnormal
Congestive Cardiomyopathy
Deafness
Dental Caries
Dilatation Ventricular
Dry Mouth
Dyspnoea
Ejection Fraction Decreased
Electrocardiogram T Wave Inversion
Fatigue
Feeling Abnormal
Gallop Rhythm Present
Keratoconjunctivitis Sicca
Leukocytoclastic Vasculitis
Loss Of Consciousness
Pruritus
Punctate Keratitis
Pyrexia
Retinal Pigment Epitheliopathy
Sjogren's SyndromeWhat is Sjogren's syndrome?
Syncope
Urticaria
Deferoxamine 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 Deferoxamine 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!