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Jurnista Side Effects

Report Jurnista Side Effects

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

Examples: headache, dizziness


The most commonly reported Jurnista side effects are:
CONSTIPATION (11 reports)
Severe Loss Of Appetite (9 reports)
Tired (9 reports)
Nausea (8 reports)
Weight Gain (7 reports)
Gastritis Acuta (5 reports)
Crying (3 reports)
Crying, Sweating, Depression (3 reports)
Depression (3 reports)
Sleeplessness (3 reports)
Sweating (3 reports)
Swolen Feet (3 reports)

If you have experienced a side effect listed above, you can check a box to report it.


View a complete list of Jurnista side effects or compare Jurnista side effects

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 (eg, physician, pharmacist). Your health care provider can provide additional clinical information and complete a copy of the side effect reporting form.

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.

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Jurnista Side Effects Reported to FDA

The following Jurnista 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 Jurnista 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.
Metastases To Bone, Metastases To Kidney, Respiratory Failure, Neoplasm Malignant
on Jul 15, 2013 Male from IT , 87 years of age, was diagnosed with and was treated with Jurnista. Directly after, patient experienced the unwanted or unexpected Jurnista side effects: metastases to bone, metastases to kidney, respiratory failure, neoplasm malignant. Jurnista dosage: N/A.
Associated medications used:
  • Durogesic
  • Contramal
  • Deltacortene
  • Lanoxin
  • Cardioaspirin
  • Portex
  • Lixidol
  • Enantone
Patient was hospitalized.

Hepatic Enzyme Increased
Patient was taking Jurnista. Patient felt the following Jurnista side effects: hepatic enzyme increased on Sep 11, 2012 from AU Additional patient health information: Female , 75 years of age, was diagnosed with and. Jurnista dosage: N/A.

Disorientation, Altered State Of Consciousness, Joint Effusion, Speech Disorder, Weight Decreased, Gastrointestinal Disorder, Urosepsis, Confusional State
Adverse event was reported on May 13, 2011 by a Female taking Jurnista (Dosage: N/A) . Location: GERMANY , weighting 187.4 lb, After Jurnista was administered, patient encountered several Jurnista side effects: disorientation, altered state of consciousness, joint effusion, speech disorder, weight decreased, gastrointestinal disorder, urosepsis, confusional state.
Multiple concurrent drugs taken:
  • Pantoprazol
  • Glucocorticoids (10 Mg Per Day)
  • Ciprofloxacin
  • Calcilac Kt (500mg/400 Once Per Day)
  • Arcoxia 60
  • Bisoprolol Fumarate
  • Iron-(ii)-glycinsulfat Complex(ferrosanol Duodenal 100mg Capsules))
  • Mtx (Per Week)
Patient was hospitalized.

Asthenia, Bile Duct Cancer, Ileus Spastic
on Jan 29, 2010 Male from KOREA, REPUBLIC OF , weighting 119.5 lb, was treated with Jurnista. Directly after, patient experienced the unwanted or unexpected Jurnista side effects: asthenia, bile duct cancer, ileus spastic. Jurnista dosage: N/A. Patient was hospitalized.


Asthenia, Ileus Spastic
on Jan 11, 2010 Male from KOREA, REPUBLIC OF , weighting 119.5 lb, was treated with Jurnista. Patient felt the following Jurnista side effects: asthenia, ileus spastic. Jurnista dosage: N/A. Patient was hospitalized.

Cardiac Failure, Disorientation
Patient was taking Jurnista. After Jurnista was administered, patient encountered several Jurnista side effects: cardiac failure, disorientation on Jul 21, 2009 from GERMANY Additional patient health information: Male , 40 years of age, . Jurnista dosage: N/A.

Cardiac Failure, Disorientation
Adverse event was reported on Jul 21, 2009 by a Male taking Jurnista (Dosage: N/A) . Location: GERMANY , 40 years of age, Directly after, patient experienced the unwanted or unexpected Jurnista side effects: cardiac failure, disorientation.

Accidental Overdose, Dyskinesia
on May 14, 2009 Male from SWITZERLAND , weighting 156.5 lb, was treated with Jurnista. Patient felt the following Jurnista side effects: accidental overdose, dyskinesia. Jurnista dosage: N/A.

Disorientation, Dyskinesia, Muscle Spasms, Myoclonus, Withdrawal Syndrome
on Apr 20, 2009 Female from SPAIN , 49 years of age, weighting 99.21 lb, was treated with Jurnista. After Jurnista was administered, patient encountered several Jurnista side effects: disorientation, dyskinesia, muscle spasms, myoclonus, withdrawal syndrome. Jurnista dosage: N/A. Patient was hospitalized.

Disorientation, Dyskinesia, Muscle Spasms, Myoclonus, Withdrawal Syndrome
Patient was taking Jurnista. Directly after, patient experienced the unwanted or unexpected Jurnista side effects: disorientation, dyskinesia, muscle spasms, myoclonus, withdrawal syndrome on Apr 14, 2009 from SPAIN Additional patient health information: Female , 49 years of age, weighting 99.21 lb, . Jurnista dosage: N/A. Patient was hospitalized.

Convulsion, Disorientation, Dyskinesia, Withdrawal Syndrome
Adverse event was reported on Apr 01, 2009 by a Female taking Jurnista (Dosage: N/A) . Location: SPAIN , 49 years of age, Patient felt the following Jurnista side effects: convulsion, disorientation, dyskinesia, withdrawal syndrome. Patient was hospitalized.

Accidental Overdose, Respiratory Failure, Restlessness
on Feb 07, 2008 Male from GERMANY , 85 years of age, was diagnosed with and was treated with Jurnista. After Jurnista was administered, patient encountered several Jurnista side effects: accidental overdose, respiratory failure, restlessness. Jurnista dosage: N/A.
Multiple concurrent drugs taken:
  • Duragesic-100


Depressed Level Of Consciousness, Feeding Tube Complication, Inadequate Analgesia, Oral Intake Reduced, Respiratory Failure, Respiratory Paralysis, Restlessness
on Apr 24, 2007 Male from GERMANY , 85 years of age, was diagnosed with and was treated with Jurnista. Directly after, patient experienced the unwanted or unexpected Jurnista side effects: depressed level of consciousness, feeding tube complication, inadequate analgesia, oral intake reduced, respiratory failure, respiratory paralysis, restlessness. Jurnista dosage: N/A.
Associated medications used:
  • Duragesic-100


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


    Track Online

  • User Sign In
  • Register to track your side effects

  • 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.

    Discuss Jurnista Side Effects

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