Recormon Side Effects

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Recormon adverse events reported to FDA.

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

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FDA Adverse Reports: 2. View All

Recormon FDA safety alerts: No

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

4784231-7 | Aseptic Necrosis Bone, Jaw Disorder, Osteonecrosis
on Apr 17, 2005 Female patient from ISRAEL , 82 years of age, was diagnosed with multiple myeloma (What is multiple myeloma?) and was treated with Recormon (View Usage). Patient experienced the following unwanted or unexpected effects: aseptic necrosis bone, jaw disorder, osteonecrosis (What is osteonecrosis?). Recormon dosage: . During the same period patient was treated with AREDIA (90 Mg, Qmo) (View Aredia Review and Aredia Label ).

4674407-1 | Aseptic Necrosis Bone
Patient was taking Recormon (View Usage). Patient had the following side effects: aseptic necrosis bone on Apr 17, 2005 from Additional patient health information: Female patient , 82 years of age, was diagnosed with multiple myeloma (What is multiple myeloma?) and. Recormon dosage: . During the same period patient was treated with AREDIA (90 Mg, Qmo) (View Aredia Review and Aredia Label ).

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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 Recormon 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 Recormon quality problem: suspected counterfeit product, potentially contaminated product indicated by suspicious odor or unusual color, inaccurate or unreadable product labeling
3. Potential Recormon 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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RECORMON Side Effects

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Recormon adverse events reported to FDA.

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Aseptic Necrosis Bone
Jaw Disorder
Osteonecrosis	What is Osteonecrosis?

RECORMON Side Effects

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Recormon adverse events reported to FDA.

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Recormon Adverse Effect Reports (FDA)

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Recormon Reactions