Tertensif Side Effects

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Tertensif adverse events reported to FDA.

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

Summary

FDA Adverse Reports: 2. View All

Tertensif FDA safety alerts: No

Reported hospitalizations: 3

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

6197509-X | Angina Pectoris, Hypokalaemia
on May 13, 2009 Female patient from SPAIN , 76 years of age, was diagnosed with hypertension and was treated with Tertensif (View Usage). Patient experienced the following unwanted or unexpected effects: angina pectoris, hypokalaemia. Tertensif dosage: . Patient was hospitalized.

5042723-X | Confusional State, Hyponatraemia
Patient was taking Tertensif (View Usage). Patient had the following side effects: confusional state, hyponatraemia on Jun 26, 2006 from Additional patient health information: Female patient , 69 years of age, was diagnosed with hypertension, epilepsy (What is epilepsy?) and. Tertensif dosage: . During the same period patient was treated with TRILEPTAL (View Trileptal Review and Trileptal 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 Tertensif 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 Tertensif quality problem: suspected counterfeit product, potentially contaminated product indicated by suspicious odor or unusual color, inaccurate or unreadable product labeling
3. Potential Tertensif 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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	Yes, Severe
	Yes, Moderate
	Yes, Minor
	No

	Exceeded Expectations
	Effective
	Somewhat Effective
	Not Effective

TERTENSIF Side Effects

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Tertensif adverse events reported to FDA.

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TERTENSIF Side Effects

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Detailed Reporting will help others get complete information and find alternative treatments to avoid or reduce side effects associated with it.

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Tertensif adverse events reported to FDA.

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Tertensif Adverse Effect Reports (FDA)

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Tertensif Reactions