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Imurek adverse events reported to FDA.

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Summary

FDA Adverse Reports: 4. View All

Imurek FDA safety alerts: No

Reported hospitalizations: 2

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Often additional risks of using a medication, such as Imurek, 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 Imurek users, Learn more about unwanted side effects & find ways to reduce them. Browse Imurek Adverse Reports reported to FDA and participate in Imurek discussion, find alternative treatments and find ways to avoid or reduce risks associated with using Imurek. 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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Imurek Adverse Effect Reports (FDA)

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6275800-6 | Gastrointestinal Haemorrhage
on Dec 11, 2008 Male patient from SWITZERLAND , 65 years of age, was diagnosed with crohn's disease (What is crohn's disease?), peripheral vascular disorder and was treated with Imurek (View Usage). Patient experienced the following unwanted or unexpected effects: gastrointestinal haemorrhage. Imurek dosage: . During the same period patient was treated with ASPIRIN (View Aspirin Review and Aspirin Label ), CALCORT (View Calcort Review and Calcort Label ), PLAVIX (View Plavix Review and Plavix Label ). Patient was hospitalized.

5427579-5 | Congenital Genitourinary Abnormality, Renal Disorder
Patient was taking Imurek (View Usage). Patient had the following side effects: congenital genitourinary abnormality, renal disorder on Aug 17, 2007 from SWITZERLAND Additional patient health information: Female patient , weighting 7.94 lb, was diagnosed with myasthenia gravis and. Imurek dosage: 175mg Per Day. During the same period patient was treated with PREDNISOLONE (15mg Per Day) (View Prednisolone Review and Prednisolone Label ), ACTONEL (35mg Weekly) (View Actonel Review and Actonel Label ), PAROXETINE (20mg Per Day) (View Paroxetine Review and Paroxetine Label ).

5423695-2 | Congenital Genitourinary Abnormality
Adverse event was reported on Aug 17, 2007 by a Female patient taking Imurek (View Usage) (Dosage: 175mg Per Day) was diagnosed with myasthenia gravis and. Location: SWITZERLAND , 23 years of age, After Imurek was administered, patient had the following side effects: congenital genitourinary abnormality. During the same period patient was treated with PREDNISOLONE (15mg Per Day) (View Prednisolone Review and Prednisolone Label ), ACTONEL (35mg Weekly) (View Actonel Review and Actonel Label ), PAROXETINE (20mg Per Day) (View Paroxetine Review and Paroxetine Label ).

4818319-9 | Alanine Aminotransferase Increased, Aspartate Aminotransferase Increased, Bile Duct Stone, Blood Alkaline Phosphatase Increased, Blood Bilirubin Increased, Blood Creatinine Increased, C-reactive Protein Increased, Choledocholithotomy, Cholelithiasis
on Oct 28, 2005 Male patient from SWITZERLAND , 68 years of age, was diagnosed with renal transplant and was treated with Imurek (View Usage). Patient experienced the following unwanted or unexpected effects: alanine aminotransferase increased, aspartate aminotransferase increased, bile duct stone, blood alkaline phosphatase increased, blood bilirubin increased, blood creatinine increased, c-reactive protein increased, choledocholithotomy, cholelithiasis. Imurek dosage: 75 Mg/d. During the same period patient was treated with ASPIRIN (100 Mg/d) (View Aspirin Review and Aspirin Label ), ZOCOR (20 Mg/d) (View Zocor Review and Zocor Label ), NORVASC (5 Mg/d) (View Norvasc Review and Norvasc Label ), CO RENITEN (1 Tab/d) (View Co-reniten Review and Co-reniten Label ), NEXIUM (40 Mg/d) (View Nexium Review and Nexium Label ), HEPARIN (10000 Iu/d) (View Heparin Review and Heparin Label ), SANDIMMUNE (100 Mg/d) (View Sandimmune Review and Sandimmune Label ), TAZOBAC (4.5 G, Tid) (View Tazobac Review and Tazobac Label ). Patient was hospitalized.


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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 Imurek 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 Imurek quality problem: suspected counterfeit product, potentially contaminated product indicated by suspicious odor or unusual color, inaccurate or unreadable product labeling
3. Potential Imurek 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 IMUREK (1 Df, Bid) (View Imurek Review and Imurek Label ), SANDIMMUNE (35 Mg, Bid) (View Sandimmune Review and Sandimmune Label ).

During the same period patient was treated with IMUREK (View Imurek Review and Imurek Label ), PREDNISOLONE (View Prednisolone Review and Prednisolone Label ), BELOC ZOK (1 Df ...

Ikorel Side Effects - Complete Patient's Guide | User Reviews: Male patient, 80 years of age, took Ikorel |Bad Neck Tightness Hospitalization|Dry Mouth|Slight Light ...

... Actonel Review and Actonel Label ), CLEXANE (View Clexane Review and Clexane Label ), FENTANYL (View Fentanyl Review and Fentanyl Label ), IMUREK /00001501/ (View Imurek ...

... Perenterol /gfr/ Label ), IMUREK /GFR/ (View Imurek /gfr/ Review and Imurek ...

During the same period patient was treated with IMUREK (View Imurek Review and Imurek Label ), PREDNISOLONE (View Prednisolone Review and Prednisolone Label ), BELOC ZOK ...

... Cyclosporine Review and Cyclosporine Label ), PREDNISONE TAB (View Prednisone Tab Review and Prednisone Tab Label ), IMUREK (View Imurek Review and Imurek Label ), METOPROLOL ...

During the same period patient was treated with IMUREK (100 Mg, Daily (1/d)) (View Imurek Review and Imurek Label ), PREDNISON (20 Mg, Daily (1/d)) (View Prednison Review and ...

... CITALOPRAM HYDROBROMIDE (View Citalopram Hydrobromide Review and Citalopram Hydrobromide Label ), DIAMICRON (View Diamicron Review and Diamicron Label ), IMUREK (View Imurek ...

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Imurek Reactions
Alanine Aminotransferase Increased
Aspartate Aminotransferase Increased
Bile Duct Stone
Blood Alkaline Phosphatase Increased
Blood Bilirubin Increased
Blood Creatinine Increased
C-reactive Protein Increased
Choledocholithotomy
Cholelithiasis
Congenital Genitourinary Abnormality
Gastrointestinal Haemorrhage
Renal Disorder
Imurek 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 Imurek 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!