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Urinorm adverse events reported to FDA.

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Summary

FDA Adverse Reports: 5. View All

Urinorm FDA safety alerts: No

Reported deaths: 2

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Often additional risks of using a medication, such as Urinorm, become known after product is used by a larger number of patients, for a longer period of time, and by patients with different health characteristics from those studied before drug approval. This page allows You to Find answers and discuss health symptoms with other Urinorm users, Learn more about unwanted side effects & find ways to reduce them. Browse Urinorm Adverse Reports reported to FDA and participate in Urinorm discussion, find alternative treatments and find ways to avoid or reduce risks associated with using Urinorm. You can also Post a question to users community or Ask a Doctor. PatientsVille.com is Your Complete Guide to all common, undocumented and undisclosed side effects associated with drugs and vaccines. Browse More Drug Reports Here: A  B  C  D  E  F  G  H  I  J  K  L  M  N  O  P  Q  R  S  T  U  V  W  X  Y  Z

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Urinorm Adverse Effect Reports (FDA)

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5802320-2 | Pneumonia, Renal Impairment
on Jun 24, 2008 Male patient from JAPAN , weighting 154.3 lb, was diagnosed with haemorrhage, cerebral ischaemia and was treated with Urinorm (View Usage). Patient experienced the following unwanted or unexpected effects: pneumonia (What is pneumonia?), renal impairment. Urinorm dosage: 50 Mg. During the same period patient was treated with OMEPRAL (10 Mg) (View Omepral Review and Omepral Label ), CINAL (3 Mg) (View Cinal Review and Cinal Label ), ALINAMIN F (25 Mg) (View Alinamin F Review and Alinamin F Label ), CLOPIDOGREL (View Clopidogrel Review and Clopidogrel Label ), MICARDIS (View Micardis Review and Micardis Label ).

5752649-1 | Blood Creatine Phosphokinase Increased
Patient was taking Urinorm (View Usage). Patient had the following side effects: blood creatine phosphokinase increased on May 21, 2008 from JAPAN Additional patient health information: Male patient , weighting 172.0 lb, was diagnosed with hypertension, hyperlipidaemia, lacunar infarction and. Urinorm dosage: 200 Mg. During the same period patient was treated with OLMETEC (40 Mg) (View Olmetec Review and Olmetec Label ), PANALDINE (200 Mg) (View Panaldine Review and Panaldine Label ), MEVALOTIN (40 Mg) (View Mevalotin Review and Mevalotin Label ), CLOPIDOGREL (View Clopidogrel Review and Clopidogrel Label ).

5684857-2 | Renal Impairment
Adverse event was reported on Mar 25, 2008 by a Male patient taking Urinorm (View Usage) (Dosage: 50 Mg) was diagnosed with haemorrhage, cerebral ischaemia and. Location: JAPAN , weighting 154.3 lb, After Urinorm was administered, patient had the following side effects: renal impairment. During the same period patient was treated with OMEPRAL (10 Mg) (View Omepral Review and Omepral Label ), CINAL (3 Mg) (View Cinal Review and Cinal Label ), ALINAMIN F (25 Mg) (View Alinamin F Review and Alinamin F Label ), CLOPIDOGREL (View Clopidogrel Review and Clopidogrel Label ).

5258604-2 | Alanine Aminotransferase Increased, Aspartate Aminotransferase Increased, Blood Alkaline Phosphatase Increased, Blood Bilirubin Increased, Gamma-glutamyltransferase Increased, Liver Disorder
on Mar 01, 2007 Male patient from JAPAN , 50 years of age, was treated with Urinorm (View Usage). Patient experienced the following unwanted or unexpected effects: alanine aminotransferase increased, aspartate aminotransferase increased, blood alkaline phosphatase increased, blood bilirubin increased, gamma-glutamyltransferase increased, liver disorder. Urinorm dosage: . During the same period patient was treated with URALYT (View Uralyt Review and Uralyt Label ), DICLOFENAC SODIUM (View Diclofenac Sodium Review and Diclofenac Sodium Label ).


5252541-5 | Liver Disorder
on Feb 21, 2007 Male patient from JAPAN , 50 years of age, was treated with Urinorm (View Usage). Patient had the following side effects: liver disorder. Urinorm dosage: . During the same period patient was treated with URALYT (View Uralyt Review and Uralyt Label ), VOLTAREN (View Voltaren Review and Voltaren Label ).


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Urinorm Questions, Answers, Feedback and Comments

Comments to date: 1. Page 1 of 1.

dr.parmod kataria   delhi

6:29am on Friday, January 29th, 2010

working n salt in uniform

To find out about documented side effects or safety concerns read either the drug label or the drug's package insert. You may also want to speak with your pharmacist or healthcare provider. All medicines have benefits and risks. The risks are the chances that something unwanted or unexpected could happen to you when you use them. You can protect yourself by searching summaries of recent safety alerts, adverse reports. Sometimes there are risks that only come to light after a medical product gets on the market and is used in a larger number of patients, for a longer period of time, and in patients whose health characteristics are different from those of the patients studied before approval.

Be aware of the following potential Urinorm risks to be aware of: 1. Watch for any Serious adverse events, such as life-threatening situation, which can require an admission to hospital or longer-than-expected hospital stay, permanent disability, birth defect, miscarriage, stillbirth, or birth with serious disease requires medical care to prevent permanent damage
2. Any potential Urinorm quality problem: suspected counterfeit product, potentially contaminated product indicated by suspicious odor or unusual color, inaccurate or unreadable product labeling
3. Potential Urinorm use error: mixing up products with similar drug names or packaging, taking wrong dose of a drug because of confusing dosing instructions on label
4. When applicable, Problems with different manufacturer of same medicine: not getting same results from a generic drug as a brand name drug, or from another generic

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During the same period patient was treated with URINORM (View Urinorm Review and ... canadiol Episodes: 1: Diagnosed with major depression.Side effects: cardiac failure ...

During the same period patient was treated with GASTROM (View Gastrom Review and Gastrom Label ), URINORM (View Urinorm Review and Urinorm Label ), BLOPRESS (View Blopress ...

Report a Drug Side Effect. ... This anonymous Drug Side Effect Survey has 13 questions and takes less than 2 minutes to complete.

During the same period patient was treated with URINORM (2 Df, Daily) (View Urinorm Side Effects and Urinorm Label ), INFLUENZA HA VACCINE (Unk) (View Influenza Ha Vaccine ...

During the same period patient was treated with URINORM (View Urinorm Review and Urinorm Label ), DIOVAN (80 Mg/day) (View Diovan Review and Diovan Label ).

... Clarithromycin Review and Clarithromycin Label ), MUCOSOLATE (View Mucosolate Review and Mucosolate Label ), URINORM (View Urinorm Review and Urinorm Label ).

... treated with BETAMETHASONE (View Betamethasone Review and Betamethasone Label ), GASTER D (View Gaster D Review and Gaster D Label ), URINORM (View Urinorm Review and Urinorm ...

During the same period patient was treated with NORVASC (5 Mg) (View Norvasc Review and Norvasc Label ), FLUITRAN (1 Mg) (View Fluitran Review and Fluitran Label ), URINORM ...

During the same period patient was treated with AMLODIN (Unk) (View Amlodin Review and Amlodin Label ), ASPIRIN (View Aspirin Review and Aspirin Label ), URINORM (View Urinorm ...

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Urinorm Reactions
Alanine Aminotransferase Increased
Aspartate Aminotransferase Increased
Blood Alkaline Phosphatase Increased
Blood Bilirubin Increased
Blood Creatine Phosphokinase Increased
Gamma-glutamyltransferase Increased
Liver Disorder
PneumoniaWhat is Pneumonia?
Renal Impairment
Urinorm Side Effects Notice - The material on this site is for informational purposes only, and is not a substitute for medical advice, diagnosis or treatment provided by a qualified health care provider. PatientsVille.com does not provide medical advice, diagnosis or treatment. The information regarding Urinorm adverse reports, reviews and polls contained on PatientsVille.com site has not been scientifically or otherwise verified as to a cause and effect relationship and cannot be used to estimate the incidence of adverse drug reactions or for establishing or changing of patient treatments. Thank you for visiting Patientsville.com!