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after my 3rd cycle of granocyte had finished. the following eveing i experienced ...Keep Reading

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Granocyte adverse events reported to FDA.

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Summary

FDA Adverse Reports: 3. View All

Granocyte FDA safety alerts: No

Reported deaths: 2

Reported hospitalizations: 1

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1Leukocytosis
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Often additional risks of using a medication, such as Granocyte, 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 Granocyte users, Learn more about unwanted side effects & find ways to reduce them. Browse Granocyte Adverse Reports reported to FDA and participate in Granocyte discussion, find alternative treatments and find ways to avoid or reduce risks associated with using Granocyte. 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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Granocyte Adverse Effect Reports (FDA)

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6401617-5 | Interstitial Lung Disease
on Jul 23, 2009 Male patient from , 72 years of age, was diagnosed with neutropenia, sarcoma and was treated with Granocyte (View Usage). Patient experienced the following unwanted or unexpected effects: interstitial lung disease. Granocyte dosage: Dose: Unk. During the same period patient was treated with TAXOTERE (View Taxotere Review and Taxotere Label ), GEMZAR (View Gemzar Review and Gemzar Label ).

6295311-1 | Interstitial Lung Disease
Patient was taking Granocyte (View Usage). Patient had the following side effects: interstitial lung disease on Jul 23, 2009 from Additional patient health information: Male patient , 72 years of age, was diagnosed with neutropenia, sarcoma and. Granocyte dosage: Dose: Unk. During the same period patient was treated with TAXOTERE (View Taxotere Review and Taxotere Label ), GEMZAR (View Gemzar Review and Gemzar Label ), MEDROL (Dose: Unk) (View Medrol Review and Medrol Label ), ZOPHREN /00955301/ (Dose: Unk) (View Zophren /00955301/ Review and Zophren /00955301/ Label ), MOTILYO (Dose: Unk) (View Motilyo Review and Motilyo Label ), DUPHALAC (Dose: Unk) (View Duphalac Review and Duphalac Label ).

5101445-7 | Cardiac Arrest, Cardiac Failure, Ejection Fraction Decreased, Incorrect Dose Administered
Adverse event was reported on Aug 31, 2006 by a Female patient taking Granocyte (View Usage) (Dosage: ) was diagnosed with agranulocytosis, acute myeloid leukaemia, vomiting, nausea (What is nausea?), gout (What is gout?) and. Location: FRANCE , weighting 22.05 lb, After Granocyte was administered, patient had the following side effects: cardiac arrest (What is cardiac arrest?), cardiac failure, ejection fraction decreased, incorrect dose administered. During the same period patient was treated with FLUDARABINE (View Fludarabine Review and Fludarabine Label ), DAUNOXOME (View Daunoxome Review and Daunoxome Label ), ZOPHREN (View Zophren Review and Zophren Label ), ARACYTINE (View Aracytine Review and Aracytine Label ), FASTURTEC (View Fasturtec Review and Fasturtec 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 Granocyte 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 Granocyte quality problem: suspected counterfeit product, potentially contaminated product indicated by suspicious odor or unusual color, inaccurate or unreadable product labeling
3. Potential Granocyte 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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Granocyte Reactions
Cardiac ArrestWhat is Cardiac arrest?
Cardiac Failure
Ejection Fraction Decreased
Incorrect Dose Administered
Interstitial Lung Disease
Granocyte 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 Granocyte 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!