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Granulokine adverse events reported to FDA.

Have You Experienced unusual Granulokine symptoms? PatientsVille.com collects and analyzes Granulokine side effect and adverse reports submitted by Granulokine users, such as .

Summary

FDA Adverse Reports: 9. View All

Granulokine FDA safety alerts: No

Reported hospitalizations: 2

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

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6431593-0 | Neutrophil Count Decreased
on Oct 12, 2009 Male patient from BRAZIL , weighting 103.6 lb, was diagnosed with neutropenia and was treated with Granulokine (View Usage). Patient experienced the following unwanted or unexpected effects: neutrophil count decreased. Granulokine dosage: .

6284470-2 | Alanine Aminotransferase Increased, Anaemia, Aspartate Aminotransferase Increased, Blood Lactate Dehydrogenase Increased, Thrombocytopenia, White Blood Cell Count Decreased
Patient was taking Granulokine (View Usage). Patient had the following side effects: alanine aminotransferase increased, anaemia, aspartate aminotransferase increased, blood lactate dehydrogenase increased, thrombocytopenia, white blood cell count decreased on Jul 17, 2009 from ITALY Additional patient health information: Female patient , weighting 68.34 lb, was diagnosed with neutropenia and. Granulokine dosage: . During the same period patient was treated with ZYLORIC (View Zyloric Review and Zyloric Label ), MYCOSTATIN (View Mycostatin Review and Mycostatin Label ). Patient was hospitalized.

5757403-2 | Eosinophilia
Adverse event was reported on May 20, 2008 by a Male patient taking Granulokine (View Usage) (Dosage: ) was diagnosed with neutropenia and. Location: BRAZIL , child 8 years of age, After Granulokine was administered, patient had the following side effects: eosinophilia.

5689111-0 | Nephrolithiasis, Renal Disorder In Pregnancy
on Mar 17, 2008 Female patient from GERMANY , 22 years of age, weighting 147.7 lb, was diagnosed with neutropenia and was treated with Granulokine (View Usage). Patient experienced the following unwanted or unexpected effects: nephrolithiasis, renal disorder in pregnancy. Granulokine dosage: . During the same period patient was treated with VITAMINS WITH MINERALS (View Vitamins With Minerals Review and Vitamins With Minerals Label ), FISH OIL (View Fish Oil Review and Fish Oil Label ).


5602799-5 | Anaemia, Bacterial Toxaemia, Blood Creatinine Increased, Chills, Hepatic Enzyme Abnormal, Hyperpyrexia, Hypokalaemia, Infection, Infusion Site Reaction
on Jan 11, 2008 Male patient from ITALY , 36 years of age, was diagnosed with neutropenia and was treated with Granulokine (View Usage). Patient had the following side effects: anaemia, bacterial toxaemia, blood creatinine increased, chills, hepatic enzyme abnormal, hyperpyrexia, hypokalaemia, infection (What is infection?), infusion site reaction. Granulokine dosage: . During the same period patient was treated with CLOZAPINE (View Clozapine Review and Clozapine Label ), LITHIUM CARBONATE (View Lithium Carbonate Review and Lithium Carbonate Label ), CITALOPRAM HYDROBROMIDE (View Citalopram Hydrobromide Review and Citalopram Hydrobromide Label ), CLOMIPRAMINE HCL (View Clomipramine Hcl Review and Clomipramine Hcl Label ), LORAZEPAM (View Lorazepam Review and Lorazepam Label ), CIPROFLOXACIN (View Ciprofloxacin Review and Ciprofloxacin Label ), CEFOTAXIME (View Cefotaxime Review and Cefotaxime Label ). Patient was hospitalized.

5564573-8 | Caesarean Section, Nephrolithiasis, Renal Disorder In Pregnancy
Patient was taking Granulokine (View Usage). After Granulokine was administered, patient had the following side effects: caesarean section, nephrolithiasis, renal disorder in pregnancy on Dec 05, 2007 from GERMANY Additional patient health information: Female patient , 22 years of age, weighting 147.7 lb, was diagnosed with neutropenia and. Granulokine dosage: . During the same period patient was treated with VITAMINS WITH MINERALS (View Vitamins With Minerals Review and Vitamins With Minerals Label ), FISH OIL (View Fish Oil Review and Fish Oil Label ).

5481477-X | Caesarean Section, Nephrolithiasis, Renal Disorder In Pregnancy
Adverse event was reported on Sep 28, 2007 by a Female patient taking Granulokine (View Usage) (Dosage: ) was diagnosed with neutropenia and. Location: GERMANY , weighting 147.7 lb, Patient experienced the following unwanted or unexpected effects: caesarean section, nephrolithiasis, renal disorder in pregnancy. During the same period patient was treated with VITAMINS WITH MINERALS (View Vitamins With Minerals Review and Vitamins With Minerals Label ), FISH OIL (View Fish Oil Review and Fish Oil Label ).

5343789-X | Asthenia, Dizziness, Dyspnoea, Influenza Like Illness, Pyrexia, White Blood Cell Count Decreased
on May 24, 2007 Male patient from BRAZIL , weighting 189.6 lb, was treated with Granulokine (View Usage). Patient had the following side effects: asthenia, dizziness (What is dizziness?), dyspnoea, influenza like illness, pyrexia, white blood cell count decreased. Granulokine dosage: .

5264923-6 | Abdominal Pain Upper, Neck Pain, Pain In Extremity, Pharyngeal Oedema, Swelling Face
on Feb 27, 2007 Female patient from BRAZIL , 24 years of age, weighting 103.6 lb, was diagnosed with neutropenia and was treated with Granulokine (View Usage). After Granulokine was administered, patient had the following side effects: abdominal pain upper, neck pain, pain in extremity, pharyngeal oedema, swelling face. Granulokine dosage: .


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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 Granulokine 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 Granulokine quality problem: suspected counterfeit product, potentially contaminated product indicated by suspicious odor or unusual color, inaccurate or unreadable product labeling
3. Potential Granulokine 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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(View Deltacortene Review and Deltacortene Label ), GRANULOKINE (View Granulokine Review and Granulokine Label ... Complete Guide to Endoxan Baxter Side Effects | Male ...

)During the same period patient was treated with GRANULOKINE, EPOETIN ALFA, RIBAVIRIN, CLEXANE, COUMADIN (Administered As Half And One Tablet In Alternate Days).

granulokine Episodes: 1: Diagnosed with major depression.Side effects: cardiac failure, myocarditis More: halcion Episodes: 1: Diagnosed with major depression.Side ...

)During the same period patient was treated with GRANULOKINE (View Granulokine Review and Granulokine Label ), EPOETIN ALFA (View Epoetin Alfa Review and Epoetin Alfa Label ...

granulokine Episodes: 2: Diagnosed with major depression.Side effects: cardiac failure, myocarditis More: gyno Episodes: 1: Diagnosed with major depression.Side ...

granulokine Episodes: 1: Diagnosed with major depression.Side effects: cardiac failure, myocarditis More: haldol Episodes: 2: Diagnosed with major depression.Side ...

granulokine Episodes: 1: Diagnosed with major depression.Side effects: cardiac failure, myocarditis More: halcion Episodes: 4: Diagnosed with major depression.Side ...

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Granulokine Reactions
Abdominal Pain Upper
Alanine Aminotransferase Increased
Anaemia
Aspartate Aminotransferase Increased
Asthenia
Bacterial Toxaemia
Blood Creatinine Increased
Blood Lactate Dehydrogenase Increased
Caesarean Section
Chills
DizzinessWhat is Dizziness?
Dyspnoea
Eosinophilia
Hepatic Enzyme Abnormal
Hyperpyrexia
Hypokalaemia
InfectionWhat is Infection?
Influenza Like Illness
Infusion Site Reaction
Neck Pain
Nephrolithiasis
Neutrophil Count Decreased
Pain In Extremity
Pharyngeal Oedema
Pyrexia
Renal Disorder In Pregnancy
Swelling Face
Thrombocytopenia
White Blood Cell Count Decreased
Granulokine 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 Granulokine 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!