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Kentera adverse events reported to FDA.

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Summary

FDA Adverse Reports: 3. View All

Kentera FDA safety alerts: No

Reported deaths: 2

Reported hospitalizations: 3

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

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5614864-7 | Application Site Reaction, Myalgia
on Jan 24, 2008 Female patient from UNITED KINGDOM , 37 years of age, weighting 299.8 lb, was diagnosed with urinary incontinence (What is urinary incontinence?) and was treated with Kentera (View Usage). Patient experienced the following unwanted or unexpected effects: application site reaction, myalgia. Kentera dosage: Transdermal. During the same period patient was treated with CETIRIZINE HCL (View Cetirizine Hcl Review and Cetirizine Hcl Label ), DIAZEPAM (View Diazepam Review and Diazepam Label ), MEBEVERINE (MEBEVERINE) (View Mebeverine (mebeverine) Review and Mebeverine (mebeverine) Label ), OMEPRAZOLE (View Omeprazole Review and Omeprazole Label ), PAROXETINE HCL (View Paroxetine Hcl Review and Paroxetine Hcl Label ).

5022395-0 | Intraocular Pressure Increased, Lip Blister
Patient was taking Kentera (View Usage). Patient had the following side effects: intraocular pressure increased, lip blister on May 22, 2006 from GERMANY Additional patient health information: Female patient , weighting 114.6 lb, was diagnosed with urge incontinence and. Kentera dosage: 1 Patch, Transdermal.

4838305-2 |
Adverse event was reported on Nov 09, 2005 by a Female patient taking Kentera (View Usage) (Dosage: 1 Patch, 2/week, Transdermal) was diagnosed with urge incontinence and. Location: GERMANY , 79 years of age, weighting 149.9 lb, .


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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 Kentera 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 Kentera quality problem: suspected counterfeit product, potentially contaminated product indicated by suspicious odor or unusual color, inaccurate or unreadable product labeling
3. Potential Kentera 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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Kentera Reactions
Application Site Reaction
Death
Intraocular Pressure Increased
Lip Blister
Myalgia
Kentera 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 Kentera 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!