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Ubretid Side Effects

Common Ubretid Side Effects


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

Suicide Attempt (1)
Renal Failure Acute (1)
Loss Of Consciousness (1)
Arrhythmia (1)
Blood Creatinine Increased (1)
Hypotension (1)
Contusion (1)
Blood Pressure Increased (1)
Intentional Overdose (1)


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.

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.

Ubretid Side Effects Reported to FDA

The following Ubretid 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.


The appearance of Ubretid 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.
Suicide Attempt, Intentional Overdose
This is a report of a 51-year-old patient (weight: NA) from GERMANY, suffering from the following symptoms/conditions: NA, who was treated with Ubretid (dosage: Unk, start time: Jan 01, 2012), combined with:
  • Lorazepam (Unk)
  • Pregabalin (Unk)
  • Citalopram Hydrobromide (Unk)
  • Metamizole (Unk)
  • Pantoprazole (Unk)
  • Ibuprofen (Unk)
  • Mirtazapine (Unk)
  • Lisinopril (Unk)
and developed a serious reaction and side effect(s). The consumer presented with:
  • Suicide Attempt
  • Intentional Overdose
which developed after the beginning of treatment. This case can indicate the possible existence of increased vulnerability to Ubretid treatment in patients, resulting in suicide attempt side effect.

Renal Failure Acute, Arrhythmia, Blood Creatinine Increased
This report suggests a potential Ubretid Renal Failure Acute, Arrhythmia, Blood Creatinine Increased side effect(s) that can have serious consequences. A 70-year-old male patient (weight: NA) from GERMANY was diagnosed with the following symptoms/conditions: NA and used Ubretid (dosage: NA) starting Aug 03, 2011. Soon after starting Ubretid the patient began experiencing various side effects, including:
  • Renal Failure Acute
  • Arrhythmia
  • Blood Creatinine Increased
Drugs used concurrently:
  • Simvastatin
  • Multaq
  • Pantoprazole
  • Torsemide
  • Metoprolol Tartrate (1-0-0.5 Daily)
  • Enoxaparin Sodium
  • Sertraline Hydrochloride
  • Candesartan Cilexetil/hydrochlorothiazide (Candesartan Cilexetil/hydrochlorothiazide 16 Mg/12.5 Mg; 1-0-0.5 Daily)
Although Ubretid demonstrated significant improvements in a number of clinically relevant cases, troublesome symptoms, such as renal failure acute, may still occur.

Blood Pressure Increased, Loss Of Consciousness, Hypotension, Contusion
This Blood Pressure Increased, Loss Of Consciousness, Hypotension, Contusion problem was reported by a pharmacist from JAPAN. A male patient (weight: NA) was diagnosed with the following symptoms/conditions: dysuria. On Jan 11, 2011 this consumer started treatment with Ubretid (dosage: 5 Mg, 1x/day). The following drugs were being taken at the same time: NA. When commencing Ubretid, the patient experienced the following unwanted symptoms/side effects:
  • Blood Pressure Increased
  • Loss Of Consciousness
  • Hypotension
  • Contusion
The 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 blood pressure increased, may become evident only after a product is in use by the general population.



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Keep Track of Side Effects

Note Your Observations

It is really important to keep of your 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

    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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    Ubretid Safety Alerts, Active Ingredients, Usage Information

    More About Ubretid

    Side Effects reported to FDA: 3

    Ubretid safety alerts: No

    Reported deaths: 1

    Reported hospitalizations: 1

    Latest Ubretid clinical trials

    Ubretid Reviews

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