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Neorecormon adverse events reported to FDA.

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Summary

FDA Adverse Reports: 5. View All

Neorecormon FDA safety alerts: No

Reported hospitalizations: 2

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

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6924980-5 | Nephrogenic Systemic Fibrosis
on Jul 22, 2010 Female patient from DENMARK , weighting 127.9 lb, was treated with Neorecormon (View Usage). Patient experienced the following unwanted or unexpected effects: nephrogenic systemic fibrosis. Neorecormon dosage: . During the same period patient was treated with VEPICOMBIN (View Vepicombin Review and Vepicombin Label ), C VITAMIN (View C-vitamin Review and C-vitamin Label ), CORODIL (View Corodil Review and Corodil Label ), FOLINSYRE (View Folinsyre Review and Folinsyre Label ), SIMVASTATIN (View Simvastatin Review and Simvastatin Label ), IPREN (View Ipren Review and Ipren Label ), LONGOVITAL (View Longovital Review and Longovital Label ), MAREVAN (View Marevan Review and Marevan Label ).

6698166-6 | Nephrogenic Systemic Fibrosis
Patient was taking Neorecormon (View Usage). Patient had the following side effects: nephrogenic systemic fibrosis on Apr 21, 2010 from GERMANY Additional patient health information: Female patient , weighting 143.3 lb, . Neorecormon dosage: . During the same period patient was treated with VEPICOMBIN (View Vepicombin Review and Vepicombin Label ), C VITAMIN (View C-vitamin Review and C-vitamin Label ), CORODIL (View Corodil Review and Corodil Label ), FOLINSYRE (View Folinsyre Review and Folinsyre Label ), SIMVASTATIN (View Simvastatin Review and Simvastatin Label ), IPREN (View Ipren Review and Ipren Label ), LONGOVITAL (View Longovital Review and Longovital Label ), WARFARIN SODIUM (View Warfarin Sodium Review and Warfarin Sodium Label ).

6377010-0 | Nephrogenic Systemic Fibrosis
Adverse event was reported on Sep 21, 2009 by a Female patient taking Neorecormon (View Usage) (Dosage: ) . Location: SWEDEN , weighting 143.3 lb, After Neorecormon was administered, patient had the following side effects: nephrogenic systemic fibrosis. During the same period patient was treated with VEPICOMBIN (View Vepicombin Review and Vepicombin Label ), C VITAMIN (View C-vitamin Review and C-vitamin Label ), CORODIL (View Corodil Review and Corodil Label ), FOLINSYRE (View Folinsyre Review and Folinsyre Label ), SIMVASTATIN (View Simvastatin Review and Simvastatin Label ), IPREN (View Ipren Review and Ipren Label ), LONGOVITAL (View Longovital Review and Longovital Label ), MAREVAN (View Marevan Review and Marevan Label ).

6042377-X | Malaise, Nausea, Renal Failure Chronic
on Jan 09, 2009 Male patient from GERMANY , 70 years of age, weighting 201.7 lb, was diagnosed with anaemia, hypertension, helicobacter gastritis, hypercholesterolaemia, hyperparathyroidism secondary and was treated with Neorecormon (View Usage). Patient experienced the following unwanted or unexpected effects: malaise, nausea (What is nausea?), renal failure chronic. Neorecormon dosage: 4000 Iu 2x Monthly. During the same period patient was treated with MOXONIDINE (View Moxonidine Review and Moxonidine Label ), XIPAMIDE (View Xipamide Review and Xipamide Label ), TOREM (View Torem Review and Torem Label ), PANTOZOL (View Pantozol Review and Pantozol Label ), FLUVASTATIN (View Fluvastatin Review and Fluvastatin Label ), EINSALPHA (View Einsalpha Review and Einsalpha Label ), EBRANTIL (View Ebrantil Review and Ebrantil Label ), DIOVANE (View Diovane Review and Diovane Label ). Patient was hospitalized.


5076941-1 | Hypothyroidism
on Jul 31, 2006 Female patient from FRANCE , 78 years of age, was diagnosed with anaemia, gastric ulcer, parkinson's disease (What is parkinson's disease?), epilepsy (What is epilepsy?), cerebrovascular accident and was treated with Neorecormon (View Usage). Patient had the following side effects: hypothyroidism. Neorecormon dosage: 4000 Iu. During the same period patient was treated with OMEPRAZOLE (View Omeprazole Review and Omeprazole Label ), MODOPAR (View Modopar Review and Modopar Label ), DEPAKENE (View Depakene Review and Depakene Label ), CORDARONE (View Cordarone Review and Cordarone Label ), PLAVIX (View Plavix Review and Plavix 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 Neorecormon 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 Neorecormon quality problem: suspected counterfeit product, potentially contaminated product indicated by suspicious odor or unusual color, inaccurate or unreadable product labeling
3. Potential Neorecormon 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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During the same period patient was treated with NEORECORMON (Dose Reported: 4000 U Per Week Form : Pre-filled Syringe) (View Neorecormon Review and Neorecormon Label ), ...

... 3000 Iu/week) (View Neorecormon Review and Neorecormon Label ), SOTALOL HCL (View Sotalol Hcl Review and Sotalol Hcl Label ), BIPRETERAX (View Bipreterax Review and ...

... Ramipril Label ), NEORECORMON (EPOETIN BETA) (30 Kiu; Qw; Sc) (View Neorecormon (epoetin Beta) Review and Neorecormon ...

During the same period patient was treated with OXYNORM (View Oxynorm Review and Oxynorm Label ), NEORECORMON ^ROCHE^ (Unk, Unk) (View Neorecormon ^roche^ Review and ...

Levothyroxine Sodium Review and Levothyroxine Sodium Label ), NEORECORMON (View Neorecormon Review and Neorecormon Label ), NOCTAMID (View Noctamid Review and Noctamid ...

During the same period patient was treated with NEORECORMON (View Neorecormon Review and Neorecormon Label ), LEVOCARNITINE (View Levocarnitine Review and Levocarnitine ...

... 3000 Iu/week) (View Neorecormon Review and Neorecormon Label ), SOTALOL HCL (View Sotalol Hcl Review and Sotalol Hcl Label ), BIPRETERAX (View Bipreterax Review and ...

During the same period patient was treated with NEORECORMON (3000 Iu/week) (View Neorecormon Review and Neorecormon Label ), SOTALOL HCL (View Sotalol Hcl Review and Sotalol ...

... Epirubicin Review and Epirubicin Label ), CYCLOPHOSPHAMIDE (View Cyclophosphamide Review and Cyclophosphamide Label ), NEORECORMON (View Neorecormon Review and Neorecormon ...

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Neorecormon Reactions
Hypothyroidism
Malaise
NauseaWhat is Nausea?
Nephrogenic Systemic Fibrosis
Renal Failure Chronic
Neorecormon 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 Neorecormon 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!