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Wytens adverse events reported to FDA.

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Summary

FDA Adverse Reports: 2. View All

Wytens FDA safety alerts: No

Reported hospitalizations: 1

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

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5275636-9 | Amnesia, Delirium, Memory Impairment, Road Traffic Accident
on Mar 14, 2007 Male patient from JAPAN , 56 years of age, was diagnosed with insomnia and was treated with Wytens (View Usage). Patient experienced the following unwanted or unexpected effects: amnesia, delirium, memory impairment, road traffic accident. Wytens dosage: 2 Mg. During the same period patient was treated with DIOVAN (80 Mg) (View Diovan Review and Diovan Label ), MYSLEE (10 Mg) (View Myslee Review and Myslee Label ).

4695982-7 | Blood Creatinine Increased, Blood Lactate Dehydrogenase Increased, Blood Triglycerides Increased, Blood Urea Increased, Cerebrovascular Accident, Glycosylated Haemoglobin Increased, Loss Of Consciousness, Malaise, Proteinuria
Patient was taking Wytens (View Usage). Patient had the following side effects: blood creatinine increased, blood lactate dehydrogenase increased, blood triglycerides increased, blood urea increased, cerebrovascular accident, glycosylated haemoglobin increased, loss of consciousness, malaise, proteinuria on Jun 14, 2005 from Additional patient health information: Male patient , 58 years of age, weighting 185.2 lb, was diagnosed with hypertension and. Wytens dosage: 10 Mg, Qd. During the same period patient was treated with DAONIL (View Daonil Review and Daonil Label ), DI ACTANE (200 Mg, Bid) (View Di-actane Review and Di-actane Label ), ALLOPURINOL (200 Mg, Qd) (View Allopurinol Review and Allopurinol Label ), TAREG (160 Mg, Qd) (View Tareg Review and Tareg Label ), PLAVIX (75 Mg, Qd) (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 Wytens 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 Wytens quality problem: suspected counterfeit product, potentially contaminated product indicated by suspicious odor or unusual color, inaccurate or unreadable product labeling
3. Potential Wytens 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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Wytens Reactions
Amnesia
Blood Creatinine Increased
Blood Lactate Dehydrogenase Increased
Blood Triglycerides Increased
Blood Urea Increased
Cerebrovascular Accident
Delirium
Glycosylated Haemoglobin Increased
Loss Of Consciousness
Malaise
Memory Impairment
Proteinuria
Road Traffic Accident
Wytens 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 Wytens 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!