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Ubretid Side Effects

Report Ubretid Side Effects

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

Examples: headache, dizziness


The most commonly reported Ubretid side effects are:
Sweating (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 Ubretid side effects . You can also compare Ubretid side effects or view FDA reports.

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).
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 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 identified a causal relationship between the drug and the listed risk.

Suicide Attempt, Intentional Overdose
on May 03, 2012 Patient from GERMANY , 51 years of age, was treated with Ubretid. Directly after, patient experienced the unwanted or unexpected Ubretid side effects: suicide attempt, intentional overdose. Ubretid dosage: Unk.
Associated medications used:
  • Lorazepam (Unk)
  • Pregabalin (Unk)
  • Citalopram Hydrobromide (Unk)
  • Metamizole (Unk)
  • Pantoprazole (Unk)
  • Ibuprofen (Unk)
  • Mirtazapine (Unk)
  • Lisinopril (Unk)


Renal Failure Acute, Arrhythmia, Blood Creatinine Increased
Patient was taking Ubretid. Patient felt the following Ubretid side effects: renal failure acute, arrhythmia, blood creatinine increased on Sep 05, 2011 from GERMANY Additional patient health information: Male , 70 years of age, weighting 200.8 lb, . Ubretid dosage: N/A.
Multiple prescriptions taken:
  • 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)


Blood Pressure Increased, Loss Of Consciousness, Hypotension, Contusion
Adverse event was reported on Feb 07, 2011 by a Male taking Ubretid (Dosage: 5 Mg, 1x/day) was diagnosed with and. Location: JAPAN , weighting 114.6 lb, After Ubretid was administered, patient encountered several Ubretid side effects: blood pressure increased, loss of consciousness, hypotension, contusion. 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 Ubretid

Side Effects reported to FDA: 3

Ubretid safety alerts: No

Reported deaths: 1

Reported hospitalizations: 1

Latest Ubretid clinical trials

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