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Dolcontin adverse events reported to FDA.

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Summary

FDA Adverse Reports: 2. View All

Dolcontin FDA safety alerts: No

Reported hospitalizations: 1

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1My Leggs Was Really Hurting,acing For Weeks After 6 Years Of Injections(daily).
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Often additional risks of using a medication, such as Dolcontin, 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 Dolcontin users, Learn more about unwanted side effects & find ways to reduce them. Browse Dolcontin Adverse Reports reported to FDA and participate in Dolcontin discussion, find alternative treatments and find ways to avoid or reduce risks associated with using Dolcontin. 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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Dolcontin Adverse Effect Reports (FDA)

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6866553-9 | Aphasia, Confusional State, Memory Impairment, Somnolence
on Jul 06, 2010 Female patient from UNITED STATES , 66 years of age, was treated with Dolcontin (View Usage). Patient experienced the following unwanted or unexpected effects: aphasia (What is aphasia?), confusional state, memory impairment, somnolence. Dolcontin dosage: 60 Mg, Bid. During the same period patient was treated with BISOPROLOL (Unk) (View Bisoprolol Review and Bisoprolol Label ), RAMIPRIL (Unk) (View Ramipril Review and Ramipril Label ), IMOVANE (Unk) (View Imovane Review and Imovane Label ), SYMBICORT (Unk) (View Symbicort Review and Symbicort Label ), ALVEDON (Unk) (View Alvedon Review and Alvedon Label ).

5545298-1 | Osteonecrosis
Patient was taking Dolcontin (View Usage). Patient had the following side effects: osteonecrosis (What is osteonecrosis?) on Dec 03, 2007 from NORWAY Additional patient health information: Male patient , 71 years of age, was diagnosed with metastatic pain, prostate cancer metastatic, thrombosis prophylaxis, metastases to bone and. Dolcontin dosage: 20 Mg/day. During the same period patient was treated with PARACETAMOL (1 G, Tid) (View Paracetamol Review and Paracetamol Label ), PREDNISOLONE (5mg) (View Prednisolone Review and Prednisolone Label ), ALBYL E (75 Mg/day) (View Albyl-e Review and Albyl-e Label ), ZOMETA (4 Mg Every 4 Weeks) (View Zometa Review and Zometa Label ). Patient was hospitalized and became disabled.


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