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Uralyt Side Effects

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Common Uralyt Side Effects


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

Intestinal Stenosis (2)
Melaena (2)
Renal Disorder (2)
Liver Disorder (2)
Hepatic Failure (1)
Vomiting (1)
Gamma-glutamyltransferase Increased (1)
Alanine Aminotransferase Increased (1)
Altered State Of Consciousness (1)
Toxicity To Various Agents (1)
Abdominal Pain (1)
Gait Disturbance (1)
Malignant Neoplasm Of Renal Pelvis (1)
Ileal Stenosis (1)
Hypertension (1)
Ileal Ulcer (1)
Interstitial Lung Disease (1)
Platelet Count Decreased (1)
Malaise (1)
Sepsis (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.

Uralyt Side Effects Reported to FDA



Uralyt Side Effect Report#8365408-0
Melaena, Intestinal Stenosis
This is a report of a male patient (weight: NA) from Japan, suffering from the following health symptoms/conditions: NA, who was treated with Uralyt (dosage: 9df, start time:
Jan 01, 2003), combined with:
  • Vesicare (5 Mg)
  • Elaszym (7200 Mg)
  • Mobic
  • Urocalun (2025 Mg)
  • Calbock (16 Mg)
  • Mobic
  • Loxonin
  • Aricept (5 Mg)
and developed a serious reaction and side effect(s): Melaena, Intestinal Stenosis after the beginning of treatment. This case can indicate the possible existence of increased vulnerability to Uralyt treatment in male patients, resulting in Melaena side effect. The patient was hospitalized.
Uralyt Side Effect Report#8241735-2
Cerebral Haemorrhage
This report suggests a potential Uralyt Cerebral Haemorrhage side effect(s) that can have serious consequences. A 63-year-old male patient (weight: NA) from Japan was diagnosed with the following symptoms/conditions: NA and used Uralyt (dosage: NA) starting
Jul 04, 2011. After starting Uralyt the patient began experiencing various side effects, including: Cerebral HaemorrhageAdditional drugs used concurrently:
  • Rabeprazole Sodium
  • Ketoprofen
The patient was hospitalized and became disabled. Although Uralyt demonstrated significant improvements in a number of clinically relevant cases, troublesome symptoms, such as Cerebral Haemorrhage, may still occur.
Uralyt Side Effect Report#8130250-2
Gait Disturbance, Altered State Of Consciousness, Dizziness, Vomiting, Toxicity To Various Agents, Cognitive Disorder
This Gait Disturbance problem was reported by a physician from Japan. A 73-year-old male patient (weight: NA) was diagnosed with the following symptoms/conditions: NA. On
Feb 23, 2011 this consumer started treatment with Uralyt (dosage: NA). The following drugs were being taken at the same time:
  • Atelec
  • Thiola (2000 Mg, Unk)
  • Avapro
  • Tegretol (4000mg, (5 Tablets 4 Times A Day))
When using Uralyt, the patient experienced the following unwanted symptoms/side effects: Gait Disturbance, Altered State Of Consciousness, Dizziness, Vomiting, Toxicity To Various Agents, Cognitive DisorderThe 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 Gait Disturbance, may become evident only after a product is in use by the general population.
Uralyt Side Effect Report#8031011-5
Condition Aggravated, Renal Disorder, Hypertension
This Condition Aggravated side effect was reported by a physician from Japan. A male patient (weight:NA) experienced the following symptoms/conditions: hyperuricaemia,hypercholesterolaemia.The patient was prescribed Uralyt (drug dosage: 3 G, Unk), which was initiated on
Aug 24, 2004. Concurrently used drugs:
  • Zetia (10 Mg, Unk)
  • Tanatril
  • Lansoprazole (15 Mg, Unk)
  • Tekturna (150 Mg)
  • Urinorm (100 Mg, Unk)
  • Adalat (40 Mg, Unk)
  • Losartan Potassium (Unk)
  • Atelec (20 Mg, Unk)
.After starting to take Uralyt the consumer reported adverse symptoms, such as: Condition Aggravated, Renal Disorder, HypertensionThese side effects may potentially be related to Uralyt.
Uralyt Side Effect Report#7928745-7
Intestinal Stenosis, Melaena
This is a report of a male patient (weight: NA) from Japan, suffering from the following health symptoms/conditions: NA, who was treated with Uralyt (dosage: 9df, start time:
Jan 01, 2003), combined with:
  • Calbock (16 Mg)
  • Isosorbide Dinitrate (80 Mg)
  • Isalon (900 Mg)
  • Mobic
  • Loxonin
  • Elaszym (7200 Mg)
  • Gastrozepin (225 Mg)
  • Mobic
and developed a serious reaction and side effect(s): Intestinal Stenosis, Melaena after the beginning of treatment. This case can indicate the possible existence of increased vulnerability to Uralyt treatment in male patients, resulting in Intestinal Stenosis side effect. The patient was hospitalized.
Uralyt Side Effect Report#7916823-8
Malaise, Aspartate Aminotransferase Increased, Gamma-glutamyltransferase Increased, Alanine Aminotransferase Increased, Liver Disorder
This report suggests a potential Uralyt (magnesium Prosphate, Solidago Virgaurea, Arnica Montana Extrac Malaise side effect(s) that can have serious consequences. A 43-year-old female patient (weight: NA) from Japan was diagnosed with the following symptoms/conditions: NA and used Uralyt (magnesium Prosphate, Solidago Virgaurea, Arnica Montana Extrac (dosage: NA) starting
May 14, 2011. After starting Uralyt (magnesium Prosphate, Solidago Virgaurea, Arnica Montana Extrac the patient began experiencing various side effects, including: Malaise, Aspartate Aminotransferase Increased, Gamma-glutamyltransferase Increased, Alanine Aminotransferase Increased, Liver DisorderAdditional drugs used concurrently:
  • Prednisolone
  • Probenecid
  • Lansoprazole
Although Uralyt (magnesium Prosphate, Solidago Virgaurea, Arnica Montana Extrac demonstrated significant improvements in a number of clinically relevant cases, troublesome symptoms, such as Malaise, may still occur.
Uralyt Side Effect Report#7825992-X
Conjunctival Hyperaemia
This Conjunctival Hyperaemia problem was reported by a physician from Japan. A male patient (weight: NA) was diagnosed with the following symptoms/conditions: NA. On
Jun 01, 2011 this consumer started treatment with Uralyt (dosage: NA). The following drugs were being taken at the same time:
  • Famotidine (40 Mg)
  • Pradaxa (220 Mg)
  • Enalapril Maleate (2.5 Mg)
  • Eplerenone (25 Mg)
  • Lasix (20 Mg)
  • Urinorm (25 Mg)
  • Carvedilol (5 Mg)
  • Famotidine (10 Mg)
When using Uralyt, the patient experienced the following unwanted symptoms/side effects: Conjunctival HyperaemiaAlthough all drugs are carefully tested before they are licensed for use, they carry side effect risks. Some side effects, such as Conjunctival Hyperaemia, may become evident only after a product is in use by the general population.
Uralyt Side Effect Report#7683530-9
Interstitial Lung Disease
This Interstitial Lung Disease side effect was reported by a physician from Japan. A 70-year-old male patient (weight:NA) experienced the following symptoms/conditions: hyperuricaemia,diabetes mellitus.The patient was prescribed Uralyt (drug dosage: NA), which was initiated on
May 16, 2008. Concurrently used drugs:
  • Januvia
  • Allopurinol
  • Lipitor
  • Allopurinol
  • Potassium Sodium Hydrogen Citrate
  • Actos
.After starting to take Uralyt the consumer reported adverse symptoms, such as: Interstitial Lung DiseaseThese side effects may potentially be related to Uralyt. The patient was hospitalized.
Uralyt Side Effect Report#7672794-3
Malignant Neoplasm Of Renal Pelvis
This is a report of a 66-year-old male patient (weight: NA) from Japan, suffering from the following health symptoms/conditions: NA, who was treated with Uralyt (sodium Citrate Acid, Potassium Citrate) (dosage: NA, start time:
Jan 20, 2009), combined with:
  • Crestor (rosumvastatin Calcium)
  • Metformin Hydrochloride
  • Actos (15 Mg (15 Mg,1 D) Per Oral)
  • Glucobay
  • Amaryl
and developed a serious reaction and side effect(s): Malignant Neoplasm Of Renal Pelvis after the beginning of treatment. This case can indicate the possible existence of increased vulnerability to Uralyt (sodium Citrate Acid, Potassium Citrate) treatment in male patients, resulting in Malignant Neoplasm Of Renal Pelvis side effect.
Uralyt Side Effect Report#7492031-2
Liver Disorder, Renal Disorder, Sepsis, Hepatic Failure
This report suggests a potential Uralyt Liver Disorder side effect(s) that can have serious consequences. A 63-year-old male patient (weight: NA) from Japan was diagnosed with the following symptoms/conditions: NA and used Uralyt (dosage: Unk) starting
Dec 01, 2010. After starting Uralyt the patient began experiencing various side effects, including: Liver Disorder, Renal Disorder, Sepsis, Hepatic FailureAdditional drugs used concurrently:
  • Intron A (Unk)
  • Nexavar (200 Mg, Bid)
  • Allopurinol (Unk)
The patient was hospitalized. Although Uralyt demonstrated significant improvements in a number of clinically relevant cases, troublesome symptoms, such as Liver Disorder, may still occur.
Uralyt Side Effect Report#7436146-3
Ileal Ulcer, Diarrhoea, Ileal Stenosis, Abdominal Pain
This Ileal Ulcer problem was reported by a physician from Japan. A 73-year-old male patient (weight: NA) was diagnosed with the following symptoms/conditions: NA. On NS this consumer started treatment with Uralyt (dosage: NA). The following drugs were being taken at the same time:
  • Zantac
  • Olmetec
  • Sigmart
  • Allopurinol
  • Omeprazole
  • Norvasc
  • Aspirin (Unk)
When using Uralyt, the patient experienced the following unwanted symptoms/side effects: Ileal Ulcer, Diarrhoea, Ileal Stenosis, Abdominal PainThe 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 Ileal Ulcer, may become evident only after a product is in use by the general population.
Uralyt Side Effect Report#7393029-5
Platelet Count Decreased, White Blood Cell Count Decreased
This Platelet Count Decreased side effect was reported by a physician from Japan. A male patient (weight:NA) experienced the following symptoms/conditions: hyperuricaemia,reflux oesophagitis,hypertension.The patient was prescribed Uralyt (drug dosage: NA), which was initiated on
Jun 04, 2008. Concurrently used drugs:
  • Omepral
  • Amlodin Od
  • Zyloric
.After starting to take Uralyt the consumer reported adverse symptoms, such as: Platelet Count Decreased, White Blood Cell Count DecreasedThese side effects may potentially be related to Uralyt.



The appearance of Uralyt 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.

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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.

    Uralyt 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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    Uralyt Safety Alerts, Active Ingredients, Usage Information

    NDC53145-311
    TypeHUMAN OTC DRUG
    Proprietary NameAuralyt
    NameCarbamide Peroxide
    Dosage FormLIQUID
    RouteTOPICAL
    On market since20140101
    LabelerMenper Distributors, Inc
    Active Ingredient(s)CARBAMIDE PEROXIDE
    Strength(s)7.8
    Unit(s)mg/12mL
    Pharma Class

    More About Uralyt

    Side Effects reported to FDA: 12

    Uralyt safety alerts: 2013

    Reported hospitalizations: 7

    Latest Uralyt clinical trials

    Uralyt Reviews

    No reviews, be a first to report a side effect via side effect reporting form