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Tertensif Side Effects

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Common Tertensif Side Effects


The most commonly reported Tertensif side effects (click to view or check a box to report):

Blood Pressure Decreased (2)
Angina Pectoris (2)
Hyponatraemia (2)
Blood Glucose Abnormal (2)
Transient Global Amnesia (2)
Renal Failure Chronic (2)
Nausea (2)
Headache (1)
Eye Swelling (1)
Gastritis (1)
Confusional State (1)
Hypokalaemia (1)
Condition Aggravated (1)
Oedema Peripheral (1)
Malaise (1)
Listless (1)
Pain In Extremity (1)
Sensation Of Heaviness (1)
Somnolence (1)
Swelling (1)

➢ More



If you or someone in your family has experienced a serious side effect to a health product, you are encouraged to report the experience to your health care professional (e.g. physician, pharmacist). You could also complete a copy of the side effect reporting form or report your side effect to FDA.

Tertensif Side Effects Reported to FDA



Tertensif Side Effect Report#7633055-1
Cerebrovascular Disorder
This is a report of a 69-year-old male patient (weight: NA) from Slovenia, suffering from the following health symptoms/conditions: NA, who was treated with Tertensif - Slow Release (dosage: 1.5 Mg, Unk, start time:
Mar 16, 2010), combined with:
  • Aspirin
  • Aliskiren (150 Mg, Qd)
  • Prenessa (8 Mg, Unk)
  • Edemid (40 Mg, Unk)
and developed a serious reaction and side effect(s): Cerebrovascular Disorder after the beginning of treatment. This case can indicate the possible existence of increased vulnerability to Tertensif - Slow Release treatment in male patients, resulting in Cerebrovascular Disorder side effect.
Tertensif Side Effect Report#7621651-7
Atrial Fibrillation, Angina Pectoris
This report suggests a potential Tertensif Sr Atrial Fibrillation side effect(s) that can have serious consequences. A male patient (weight: NA) from Switzerland was diagnosed with the following symptoms/conditions: NA and used Tertensif Sr (dosage: Unk) starting
Oct 14, 2010. After starting Tertensif Sr the patient began experiencing various side effects, including: Atrial Fibrillation, Angina PectorisAdditional drugs used concurrently:
  • Plavix (Unk)
  • Ramipril
  • Ranibizumab (0.5 Mg, Unk)
  • Acard (Unk)
  • Simvastatin (Unk)
The patient was hospitalized. Although Tertensif Sr demonstrated significant improvements in a number of clinically relevant cases, troublesome symptoms, such as Atrial Fibrillation, may still occur.
Tertensif Side Effect Report#7437130-6
Pain In Extremity, Eye Swelling, Blood Pressure Decreased, Transient Global Amnesia, Blood Glucose Abnormal, Oedema Peripheral, Brain Oedema
This Pain In Extremity problem was reported by a consumer or non-health professional from Poland. A 61-year-old male patient (weight: NA) was diagnosed with the following symptoms/conditions: NA. On
Jan 28, 2004 this consumer started treatment with Tertensif - Slow Release (dosage: NA). The following drugs were being taken at the same time: NA. When using Tertensif - Slow Release, the patient experienced the following unwanted symptoms/side effects: Pain In Extremity, Eye Swelling, Blood Pressure Decreased, Transient Global Amnesia, Blood Glucose Abnormal, Oedema Peripheral, Brain OedemaThe patient was hospitalized.Although all drugs are carefully tested before they are licensed for use, they carry side effect risks. Some side effects, such as Pain In Extremity, may become evident only after a product is in use by the general population.
Tertensif Side Effect Report#7277206-X
Nausea, Gastritis
This Nausea side effect was reported by a health professional from Germany. A female patient (weight:NA) experienced the following symptoms/conditions: NA.The patient was prescribed Tertensif (drug dosage: NA), which was initiated on
Aug 23, 2010. Concurrently used drugs:
  • 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))
.After starting to take Tertensif the consumer reported adverse symptoms, such as: Nausea, GastritisThese side effects may potentially be related to Tertensif. The patient was hospitalized.
Tertensif Side Effect Report#7206803-2
Transient Global Amnesia, Swelling, Blood Glucose Abnormal, Blood Pressure Decreased
This is a report of a 67-year-old male patient (weight: NA) from Poland, suffering from the following health symptoms/conditions: hypertension, who was treated with Tertensif - Slow Release (dosage: NA, start time: NS), combined with: NA. and developed a serious reaction and side effect(s): Transient Global Amnesia, Swelling, Blood Glucose Abnormal, Blood Pressure Decreased after the beginning of treatment. This case can indicate the possible existence of increased vulnerability to Tertensif - Slow Release treatment in male patients, resulting in Transient Global Amnesia side effect. The patient was hospitalized.
Tertensif Side Effect Report#6665577-4
Blood Pressure Ambulatory Increased, Listless, Malaise, Sensation Of Heaviness, Syncope
This report suggests a potential Tertensif - Slow Release Blood Pressure Ambulatory Increased side effect(s) that can have serious consequences. A 73-year-old male patient (weight: NA) from Croatia (local Name: Hrvatska) was diagnosed with the following symptoms/conditions: hypertension and used Tertensif - Slow Release (dosage: NA) starting
Feb 02, 2010. After starting Tertensif - Slow Release the patient began experiencing various side effects, including: Blood Pressure Ambulatory Increased, Listless, Malaise, Sensation Of Heaviness, SyncopeAdditional drugs used concurrently: NA. Although Tertensif - Slow Release demonstrated significant improvements in a number of clinically relevant cases, troublesome symptoms, such as Blood Pressure Ambulatory Increased, may still occur.
Tertensif Side Effect Report#6197509-X
Angina Pectoris, Hypokalaemia
This Angina Pectoris problem was reported by a physician from Spain. A 76-year-old female patient (weight: NA) was diagnosed with the following symptoms/conditions: hypertension. On
Mar 01, 2008 this consumer started treatment with Tertensif (dosage: NA). The following drugs were being taken at the same time: NA. When using Tertensif, the patient experienced the following unwanted symptoms/side effects: Angina Pectoris, HypokalaemiaThe patient was hospitalized.Although all drugs are carefully tested before they are licensed for use, they carry side effect risks. Some side effects, such as Angina Pectoris, may become evident only after a product is in use by the general population.
Tertensif Side Effect Report#5042723-X
Confusional State, Hyponatraemia
This Confusional State side effect was reported by a consumer or non-health professional from . A 69-year-old female patient (weight:NA) experienced the following symptoms/conditions: hypertension,epilepsy.The patient was prescribed Tertensif (drug dosage: NA), which was initiated on
Jan 01, 2003. Concurrently used drugs:
  • Trileptal
.After starting to take Tertensif the consumer reported adverse symptoms, such as: Confusional State, HyponatraemiaThese side effects may potentially be related to Tertensif. The patient was hospitalized.
Tertensif Side Effect Report#5016514-X
Headache, Hyponatraemia, Nausea, Somnolence
This is a report of a 70-year-old female patient (weight: NA) from , suffering from the following health symptoms/conditions: hypertension, who was treated with Tertensif - Slow Release (dosage: NA, start time: NS), combined with:
  • Quinapril
and developed a serious reaction and side effect(s): Headache, Hyponatraemia, Nausea, Somnolence after the beginning of treatment. This case can indicate the possible existence of increased vulnerability to Tertensif - Slow Release treatment in female patients, resulting in Headache side effect. The patient was hospitalized.
Tertensif Side Effect Report#4608499-2
Renal Failure Chronic
This report suggests a potential Tertensif - Slow Release Renal Failure Chronic side effect(s) that can have serious consequences. A 86-year-old female patient (weight: NA) from was diagnosed with the following symptoms/conditions: NA and used Tertensif - Slow Release (dosage: NA) starting
Nov 16, 2003. After starting Tertensif - Slow Release the patient began experiencing various side effects, including: Renal Failure ChronicAdditional drugs used concurrently:
  • Torsemide
  • Valsartan
The patient was hospitalized. Although Tertensif - Slow Release demonstrated significant improvements in a number of clinically relevant cases, troublesome symptoms, such as Renal Failure Chronic, may still occur.
Tertensif Side Effect Report#4565133-8
Condition Aggravated, Renal Failure Chronic
This Condition Aggravated problem was reported by a consumer or non-health professional from . A 86-year-old female patient (weight: NA) was diagnosed with the following symptoms/conditions: NA. On
Nov 16, 2003 this consumer started treatment with Tertensif - Slow Release (dosage: NA). The following drugs were being taken at the same time:
  • Torsemide
  • Valsartan
When using Tertensif - Slow Release, the patient experienced the following unwanted symptoms/side effects: Condition Aggravated, Renal Failure ChronicThe patient was hospitalized.Although all drugs are carefully tested before they are licensed for use, they carry side effect risks. Some side effects, such as Condition Aggravated, may become evident only after a product is in use by the general population.



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 found a causal relationship between the drug and the listed risk.


Track Your Side Effects

Note Your Observations

It is really important to keep track of your health symptoms, right from the time you start a new medicine. You can do it any way you prefer: in a notebook, in a computer file or using our online tool. You should also note down any other medicines you are taking at the same time, because there could be an interaction between these medicines.

Why Your Notes are Important

Your notes could be helpful in several ways:

  • You can use them to remind you of details that may alert your health care professional(s) to a problem
  • You will have a record to refer to in the future, in case you are ever prescribed the same medicine again

  • Log Form

    You can use the following log form to write down important information, like the date and time you experienced a side effect and your symptoms, how strong the symptoms were, and any other medicines you were using.

    Medicine Name and Dosage:
    Side Effects Scale Date & Time Other Medicine(s) or Treatment(s)
    Scale: 1 = very mild to 10 = very bad

    Side effects reports are analyzed to discover potential health product safety signals. Some important reactions may take an extremely long time to develop or occur infrequently. Continued monitoring of adverse reactions is thus essential to maintain a comprehensive safety and effectiveness profile of health products.

    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.

    Tertensif reports list potential signals of serious risks and new safety information that were identified using the FDA Adverse Event Reporting System (FAERS).
    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.

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    More About Tertensif

    Side Effects reported to FDA: 11

    Tertensif safety alerts: No

    Reported deaths: 1

    Reported hospitalizations: 5

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