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Stemgen adverse events reported to FDA.

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Summary

FDA Adverse Reports: 3. View All

Stemgen FDA safety alerts: No

Reported hospitalizations: 2

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

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5682417-0 | Blast Cell Count Increased
on Mar 12, 2008 Male patient from FRANCE , weighting 168.7 lb, was diagnosed with peripheral blood stem cell apheresis, blood stem cell harvest and was treated with Stemgen (View Usage). Patient experienced the following unwanted or unexpected effects: blast cell count increased. Stemgen dosage: . During the same period patient was treated with NEUPOGEN (View Neupogen Review and Neupogen Label ), VENTOLIN (View Ventolin Review and Ventolin Label ), ZYRTEC (View Zyrtec Review and Zyrtec Label ), RANITIDINE (View Ranitidine Review and Ranitidine Label ), VALACYCLOVIR (View Valacyclovir Review and Valacyclovir Label ), PENTACARINAT (View Pentacarinat Review and Pentacarinat Label ), ARACYTINE (View Aracytine Review and Aracytine Label ). Patient was hospitalized.

5602321-3 | Anaphylactoid Shock
Patient was taking Stemgen (View Usage). Patient had the following side effects: anaphylactoid shock on Jan 14, 2008 from FRANCE Additional patient health information: Female patient , weighting 209.4 lb, . Stemgen dosage: . During the same period patient was treated with NEUPOGEN (View Neupogen Review and Neupogen Label ).

4637713-2 | Angioneurotic Oedema
Adverse event was reported on Apr 08, 2005 by a Male patient taking Stemgen (View Usage) (Dosage: ) was diagnosed with peripheral blood stem cell apheresis and. Location: , weighting 172.0 lb, After Stemgen was administered, patient had the following side effects: angioneurotic oedema. During the same period patient was treated with NEUPOGEN (View Neupogen Review and Neupogen Label ), LANSOPRAZOLE (View Lansoprazole Review and Lansoprazole Label ), SALBUTAMOL (View Salbutamol Review and Salbutamol Label ), RANITIDINE (View Ranitidine Review and Ranitidine Label ), CETIRIZINE HCL (View Cetirizine Hcl Review and Cetirizine Hcl Label ), LEVODOPA (View Levodopa Review and Levodopa 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 Stemgen 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 Stemgen quality problem: suspected counterfeit product, potentially contaminated product indicated by suspicious odor or unusual color, inaccurate or unreadable product labeling
3. Potential Stemgen 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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Stemgen 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 Stemgen 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!