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Anagrelide adverse events reported to FDA.

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Summary

FDA Adverse Reports: 4. View All

Anagrelide FDA safety alerts: 2005

Reported deaths: 20

Reported hospitalizations: 58

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

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5122854-6 | Pruritus
on Oct 04, 2006 Male patient from UNITED STATES , weighting 220.0 lb, was treated with Anagrelide (View Usage). Patient experienced the following unwanted or unexpected effects: pruritus. Anagrelide dosage: 0.5 Mg Tid Po.

4844715-X | Ascites, Atrioventricular Block First Degree, Cardiac Disorder, Cardiac Failure Congestive, Dilatation Atrial, Dilatation Ventricular, Essential Thrombocythaemia, Haematocrit Decreased, Haemoglobin Decreased
Patient was taking Anagrelide (View Usage). Patient had the following side effects: ascites, atrioventricular block first degree, cardiac disorder, cardiac failure congestive, dilatation atrial, dilatation ventricular, essential thrombocythaemia, haematocrit decreased, haemoglobin decreased on Nov 15, 2005 from UNITED STATES Additional patient health information: Male patient , 34 years of age, was diagnosed with essential thrombocythaemia and. Anagrelide dosage: 8 Mg Qday.

4837391-3 | Renal Failure Chronic
Adverse event was reported on Nov 23, 2005 by a Female patient taking Anagrelide (View Usage) (Dosage: 14 Caps Daily 5+5+4) was diagnosed with thrombocythaemia and. Location: UNITED STATES , 67 years of age, weighting 160.0 lb, After Anagrelide was administered, patient had the following side effects: renal failure chronic. During the same period patient was treated with SYNTHROID (View Synthroid Review and Synthroid Label ), PROCRIT (View Procrit Review and Procrit Label ).

4732563-0 | Arrhythmia
on Aug 01, 2005 Male patient from UNITED STATES , 77 years of age, weighting 143.1 lb, was treated with Anagrelide (View Usage). Patient experienced the following unwanted or unexpected effects: arrhythmia (What is arrhythmia?). Anagrelide 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 Anagrelide 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 Anagrelide quality problem: suspected counterfeit product, potentially contaminated product indicated by suspicious odor or unusual color, inaccurate or unreadable product labeling
3. Potential Anagrelide 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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Anagrelide Reactions
ArrhythmiaWhat is Arrhythmia?
Ascites
Atrioventricular Block First Degree
Cardiac Disorder
Cardiac Failure Congestive
Dilatation Atrial
Dilatation Ventricular
Essential Thrombocythaemia
Haematocrit Decreased
Haemoglobin Decreased
Pruritus
Renal Failure Chronic
Anagrelide 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 Anagrelide 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!