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Tertensif Side Effects

Report Tertensif Side Effects

If you experienced any harmful or unwanted effects of Tertensif, please share your experience. This could help to raise awareness about Tertensif side effects, identify uknown risks and inform health professionals and patients taking Tertensif.

Examples: headache, dizziness


The most commonly reported Tertensif side effects are:
Big Feet (1 reports)
Big Feet And Legs (1 reports)
Dizziness (1 reports)
Legs (1 reports)

If you have experienced a side effect listed above, you can check a box to report it.


To view a complete list of submitted side effects, please follow the link Tertensif side effects . You can also compare Tertensif side effects or view FDA reports.

Tertensif Side Effects reported to FDA

The following Tertensif reports list potential signals of serious risks and new safety information that were identified using the FDA Adverse Event Reporting System (FAERS).
The FAERS is a database that contains information on adverse event and medication errors reports submitted to FDA by healthcare professionals (such as physicians, pharmacists, nurses and others), consumers (such as patients, family members, layers and others) and manufacturers.


The appearance of Tertensif on this list does not mean that FDA has concluded that the drug has the listed risk. It means that FDA has identified a potential safety issue, but it does not mean that FDA has identified a causal relationship between the drug and the listed risk.

Cerebrovascular Disorder
on Jul 19, 2011 Male from SLOVENIA , 69 years of age, was treated with Tertensif - Slow Release. Directly after, patient experienced the unwanted or unexpected Tertensif side effects: cerebrovascular disorder. Tertensif - Slow Release dosage: 1.5 Mg, Unk.
Associated medications used:
  • Aspirin
  • Aliskiren (150 Mg, Qd)
  • Prenessa (8 Mg, Unk)
  • Edemid (40 Mg, Unk)


Atrial Fibrillation, Angina Pectoris
Patient was taking Tertensif Sr. Patient felt the following Tertensif side effects: atrial fibrillation, angina pectoris on Jul 06, 2011 from SWITZERLAND Additional patient health information: Male , weighting 156.5 lb, . Tertensif Sr dosage: Unk.
Multiple prescriptions taken:
  • Plavix (Unk)
  • Ramipril
  • Ranibizumab (0.5 Mg, Unk)
  • Acard (Unk)
  • Simvastatin (Unk)
Patient was hospitalized.

Pain In Extremity, Eye Swelling, Blood Pressure Decreased, Transient Global Amnesia, Blood Glucose Abnormal, Oedema Peripheral, Brain Oedema
Adverse event was reported on Apr 18, 2011 by a Male taking Tertensif - Slow Release (Dosage: N/A) . Location: POLAND , 61 years of age, After Tertensif was administered, patient encountered several Tertensif side effects: pain in extremity, eye swelling, blood pressure decreased, transient global amnesia, blood glucose abnormal, oedema peripheral, brain oedema. Patient was hospitalized.

Nausea, Gastritis
on Jan 19, 2011 Female from GERMANY , weighting 149.9 lb, was treated with Tertensif. Directly after, patient experienced the unwanted or unexpected Tertensif side effects: nausea, gastritis. Tertensif dosage: N/A.
Associated medications used:
  • Aspenter
  • Digoxin
  • Madopar /00349201/
  • Amaryl
  • Nebivolol Hcl
  • Rivotril
  • Rotigotine (rotigotine) ((2 Mg Qd) ; (4 Mg Qd) ; (6 Mg Qd) ; (8 Mg Qd))
  • Rotigotine (rotigotine) ((2 Mg Qd) ; (4 Mg Qd) ; (6 Mg Qd) ; (8 Mg Qd))
Patient was hospitalized.


Transient Global Amnesia, Swelling, Blood Glucose Abnormal, Blood Pressure Decreased
on Dec 22, 2010 Male from POLAND , 67 years of age, was diagnosed with and was treated with Tertensif - Slow Release. Patient felt the following Tertensif side effects: transient global amnesia, swelling, blood glucose abnormal, blood pressure decreased. Tertensif - Slow Release dosage: N/A. Patient was hospitalized.

Blood Pressure Ambulatory Increased, Listless, Malaise, Sensation Of Heaviness, Syncope
Patient was taking Tertensif - Slow Release. After Tertensif was administered, patient encountered several Tertensif side effects: blood pressure ambulatory increased, listless, malaise, sensation of heaviness, syncope on Mar 24, 2010 from CROATIA (local name: Hrvatska) Additional patient health information: Male , 73 years of age, was diagnosed with and. Tertensif - Slow Release dosage: N/A.

Angina Pectoris, Hypokalaemia
Adverse event was reported on May 13, 2009 by a Female taking Tertensif (Dosage: N/A) was diagnosed with and. Location: SPAIN , 76 years of age, Directly after, patient experienced the unwanted or unexpected Tertensif side effects: angina pectoris, hypokalaemia. Patient was hospitalized.

Confusional State, Hyponatraemia
on Jun 26, 2006 Female from , 69 years of age, was diagnosed with and was treated with Tertensif. Patient felt the following Tertensif side effects: confusional state, hyponatraemia. Tertensif dosage: N/A.
Multiple prescriptions taken: Patient was hospitalized.

Headache, Hyponatraemia, Nausea, Somnolence
on May 24, 2006 Female from , 70 years of age, was diagnosed with and was treated with Tertensif - Slow Release. After Tertensif was administered, patient encountered several Tertensif side effects: headache, hyponatraemia, nausea, somnolence. Tertensif - Slow Release dosage: N/A.
Multiple concurrent drugs taken: Patient was hospitalized.

Renal Failure Chronic
Patient was taking Tertensif - Slow Release. Directly after, patient experienced the unwanted or unexpected Tertensif side effects: renal failure chronic on Jan 25, 2005 from Additional patient health information: Female , 86 years of age, . Tertensif - Slow Release dosage: N/A.
Associated medications used: Patient was hospitalized.

Condition Aggravated, Renal Failure Chronic
Adverse event was reported on Jan 25, 2005 by a Female taking Tertensif - Slow Release (Dosage: N/A) . Location: , 86 years of age, Patient felt the following Tertensif side effects: condition aggravated, renal failure chronic.
Multiple prescriptions taken: Patient was hospitalized.

Record and Track Your Side Effects

It is very important to keep track of all side effects and discuss them with your doctor. If you think you may have a medical emergency, call your doctor or 911 immediately.

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Most drugs have a large list of nonsevere or mild adverse effects which do not rule out continued usage. These effects depend on individual sensitivity, and can include nausea, dizziness, diarrhea, malaise, vomiting, headache, dermatitis, dry mouth, etc. Check commonly reported side effects . These can be considered a form of pseudo-allergic reaction, as not all users experience these effects; many users experience none at all.

You are encouraged to report negative side effects of prescription drugs to the FDA. Visit the FDA MedWatch website or call 1-800-FDA-1088.

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Safety Alerts, Active Ingredients, Usage Information

More About Tertensif

Side Effects reported to FDA: 11

Tertensif safety alerts: No

Reported deaths: 1

Reported hospitalizations: 5

Latest Tertensif clinical trials

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