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Octegra adverse events reported to FDA.

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

Summary

FDA Adverse Reports: 5. View All

Octegra FDA safety alerts: No

Reported hospitalizations: 2

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

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5336522-9 | Tendonitis
on May 23, 2007 Male patient from SPAIN , 42 years of age, weighting 147.7 lb, was diagnosed with respiratory disorder and was treated with Octegra (View Usage). Patient experienced the following unwanted or unexpected effects: tendonitis. Octegra dosage: Total Daily Dose: 400 Mg Unit Dose: 400 Mg.

5257666-6 | Tendonitis
Patient was taking Octegra (View Usage). Patient had the following side effects: tendonitis on Mar 01, 2007 from SPAIN Additional patient health information: Male patient , 42 years of age, weighting 147.7 lb, was diagnosed with respiratory disorder and. Octegra dosage: Total Daily Dose: 400 Mg Unit Dose: 400 Mg.

5199006-7 | Tendonitis
Adverse event was reported on Jan 01, 2007 by a Male patient taking Octegra (View Usage) (Dosage: Total Daily Dose: 400 Mg Unit Dose: 400 Mg) was diagnosed with respiratory disorder and. Location: SPAIN , 42 years of age, weighting 147.7 lb, After Octegra was administered, patient had the following side effects: tendonitis.

5118462-3 | Asthenia, Hypotonia, Muscular Weakness, Myalgia
on Sep 04, 2006 Male patient from ITALY , 56 years of age, was diagnosed with tonsillitis and was treated with Octegra (View Usage). Patient experienced the following unwanted or unexpected effects: asthenia, hypotonia, muscular weakness, myalgia. Octegra dosage: Total Daily Dose: 400 Mg Unit Dose: 400 Mg. Patient was hospitalized.


5100970-2 | Asthenia, Hypotonia, Muscular Weakness, Myalgia
on Sep 04, 2006 Male patient from ITALY , 56 years of age, was diagnosed with tonsillitis and was treated with Octegra (View Usage). Patient had the following side effects: asthenia, hypotonia, muscular weakness, myalgia. Octegra dosage: . 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 Octegra 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 Octegra quality problem: suspected counterfeit product, potentially contaminated product indicated by suspicious odor or unusual color, inaccurate or unreadable product labeling
3. Potential Octegra 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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