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Teveten Side Effects

Generic Name: eprosartan

Note: This page contains side effects data for the generic drug eprosartan. It is possible that some of the dosage forms included below may not apply to the brand name Teveten.

For the Consumer

Applies to eprosartan: oral tablet

As well as its needed effects, eprosartan (the active ingredient contained in Teveten) may cause unwanted side effects that require medical attention.

If any of the following side effects occur while taking eprosartan, check with your doctor immediately:

Less common
  • Burning or painful urination or changes in urinary frequency
  • cough
  • fever
  • sore throat
Rare
  • Dizziness, lightheadedness, or fainting
  • swollen face, lips, limbs, or tongue

Some eprosartan side effects may not need any medical attention. As your body gets used to the medicine these side effects may disappear. Your health care professional may be able to help you prevent or reduce these side effects, but do check with them if any of the following side effects continue, or if you are concerned about them:

Less common or rare
  • Abdominal or stomach pain
  • joint pain
  • unusual tiredness

For Healthcare Professionals

Applies to eprosartan: oral tablet

General

The most common adverse reactions were headache and unspecific gastrointestinal complaints.[Ref]

Nervous system

Very common (10% or more): Headache (up to 11%)
Common (1% to 10%): Dizziness
Frequency not reported: Ataxia, migraine, neuritis, paresthesia, somnolence, tremor, vertigo, tinnitus[Ref]

Gastrointestinal

Common (1% to 10%): Unspecific gastrointestinal complaints, abdominal pain, diarrhea, dyspepsia
Frequency not reported: Constipation, dry mouth, esophagitis, flatulence, gastritis, gastroenteritis, gingivitis, nausea, periodontitis, toothache, vomiting[Ref]

Respiratory

Common (1% to 10%): Rhinitis, upper respiratory tract infection, pharyngitis, coughing, sinusitis, dyspnea, bronchitis
Frequency not reported: Asthma, epistaxis[Ref]

Other

Common (1% to 10%): Asthenia, injury, chest pain, fatigue, pain
Uncommon (0.1% to 1%): Facial edema
Frequency not reported: Substernal chest pain, peripheral edema, fever, influenza-like symptoms, malaise[Ref]

Musculoskeletal

Common (1% to 10%): Myalgia, arthralgia, back pain
Frequency not reported: Rigors, creatine phosphokinase increased, arthritis, arthritis aggravated, arthrosis, skeletal pain, tendinitis, leg cramps[Ref]

Cardiovascular

Common (1% to 10%): Palpitation, dependent edema
Uncommon (0.1% to 1%): Hypotension
Frequency not reported: Hot flushes, angina pectoris, bradycardia, ECG abnormal, ECG specific abnormal, extrasystoles, atrial fibrillation, tachycardia, peripheral ischemia[Ref]

Hematologic

Common (1% to 10%): Neutrophils 1500/mm3 or less
Uncommon (0.1% to 1%): Hemoglobin decreased greater than 20%, WBC count of 3000/mm3 or less, platelets 100 x 10(9)/L or less
Frequency not reported: Anemia, leukopenia[Ref]

Metabolic

Common (1% to 10%): Hypertriglyceridemia
Uncommon (0.1% to 1%): Potassium 5.6 mmol/L or greater
Frequency not reported: Alcohol intolerance, anorexia, diabetes mellitus, gout, hypercholesterolemia, hyperglycemia, hyperkalemia, hypokalemia, hyponatremia[Ref]

Dermatologic

Common (1% to 10%): Allergic skin reactions
Uncommon (0.1% to 1%): Angioedema
Frequency not reported: Purpura, eczema, furunculosis, pruritus, rash, maculopapular rash, sweating increased[Ref]

Immunologic

Common (1% to 10%): Viral infection
Uncommon (0.1% to 1%): Hypersensitivity
Frequency not reported: Herpes simplex, otitis externa, otitis media[Ref]

Renal

Common (1% to 10%): BUN increased
Uncommon (0.1% to 1%): Creatinine increased
Frequency not reported: Renal calculus
Postmarketing reports: Impaired renal function, renal failure[Ref]

Genitourinary

Common (1% to 10%): Urinary tract infection
Frequency not reported: Glycosuria, albuminuria, cystitis, hematuria, micturition frequency, polyuria, urinary incontinence[Ref]

Psychiatric

Common (1% to 10%): Depression
Frequency not reported: Anxiety, insomnia, nervousness[Ref]

Hepatic

Uncommon (0.1% to 1%): ALT greater than 3.5 times the upper limit of normal
Frequency not reported: Serum glutamic oxaloacetic transaminase (SGOT) increased, serum glutamic pyruvic transaminase (SGPT) increased, ALT increased, AST increased, alkaline phosphatase increased[Ref]

Ocular

Frequency not reported: Conjunctivitis, vision abnormal, xerophthalmia[Ref]

References

1. Cerner Multum, Inc. "Australian Product Information." O 0

2. "Product Information. Teveten (eprosartan)." SmithKline Beecham, Philadelphia, PA.

3. Cerner Multum, Inc. "UK Summary of Product Characteristics." O 0

It is possible that some side effects of Teveten may not have been reported. These can be reported to the FDA here. Always consult a healthcare professional for medical advice.

Disclaimer: Every effort has been made to ensure that the information provided is accurate, up-to-date and complete, but no guarantee is made to that effect. In addition, the drug information contained herein may be time sensitive and should not be utilized as a reference resource beyond the date hereof. This material does not endorse drugs, diagnose patients, or recommend therapy. This information is a reference resource designed as supplement to, and not a substitute for, the expertise, skill , knowledge, and judgement of healthcare practitioners in patient care. The absence of a warning for a given drug or combination thereof in no way should be construed to indicate safety, effectiveness, or appropriateness for any given patient. Drugs.com does not assume any responsibility for any aspect of healthcare administered with the aid of materials provided. The information contained herein is not intended to cover all possible uses, directions, precautions, warnings, drug interactions, allergic reactions, or adverse effects. If you have questions about the substances you are taking, check with your doctor, nurse, or pharmacist.

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