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Jurnista Side Effects

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Common Jurnista Side Effects


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

Disorientation (6)
Dyskinesia (4)
Withdrawal Syndrome (3)
Respiratory Failure (3)
Cardiac Failure (2)
Accidental Overdose (2)
Ileus Spastic (2)
Asthenia (2)
Restlessness (2)
Myoclonus (2)
Muscle Spasms (2)
Bile Duct Cancer (1)
Inadequate Analgesia (1)
Confusional State (1)
Altered State Of Consciousness (1)
Feeding Tube Complication (1)
Hepatic Enzyme Increased (1)
Gastrointestinal Disorder (1)
Depressed Level Of Consciousness (1)
Convulsion (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.

Jurnista Side Effects Reported to FDA



Jurnista Side Effect Report#9399982
Metastases To Bone, Metastases To Kidney, Respiratory Failure, Neoplasm Malignant
This is a report of a 87-year-old male patient (weight: NA) from IT, suffering from the following health symptoms/conditions: pain, who was treated with Jurnista (dosage: NA, start time:
Jun 01, 2013), combined with:
  • Durogesic
  • Contramal
  • Deltacortene
  • Lanoxin
  • Cardioaspirin
  • Portex
  • Lixidol
  • Enantone
and developed a serious reaction and side effect(s): Metastases To Bone, Metastases To Kidney, Respiratory Failure, Neoplasm Malignant after the beginning of treatment. This case can indicate the possible existence of increased vulnerability to Jurnista treatment in male patients, resulting in Metastases To Bone side effect. The patient was hospitalized.
Jurnista Side Effect Report#8776924
Hepatic Enzyme Increased
This report suggests a potential Jurnista Hepatic Enzyme Increased side effect(s) that can have serious consequences. A 75-year-old female patient (weight: NA) from AU was diagnosed with the following symptoms/conditions: back pain and used Jurnista (dosage: NA) starting
Apr 07, 2011. After starting Jurnista the patient began experiencing various side effects, including: Hepatic Enzyme IncreasedAdditional drugs used concurrently: NA. Although Jurnista demonstrated significant improvements in a number of clinically relevant cases, troublesome symptoms, such as Hepatic Enzyme Increased, may still occur.
Jurnista Side Effect Report#7494383-6
Disorientation, Altered State Of Consciousness, Joint Effusion, Speech Disorder, Weight Decreased, Gastrointestinal Disorder, Urosepsis, Confusional State
This Disorientation problem was reported by a physician from Germany. A female patient (weight: NA) was diagnosed with the following symptoms/conditions: NA. On
Sep 20, 2010 this consumer started treatment with Jurnista (dosage: NA). The following drugs were being taken at the same time:
  • 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)
When using Jurnista, the patient experienced the following unwanted symptoms/side effects: Disorientation, Altered State Of Consciousness, Joint Effusion, Speech Disorder, Weight Decreased, Gastrointestinal Disorder, Urosepsis, Confusional StateThe 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 Disorientation, may become evident only after a product is in use by the general population.
Jurnista Side Effect Report#6579877-X
Asthenia, Bile Duct Cancer, Ileus Spastic
This Asthenia side effect was reported by a physician from Korea, Republic Of. A male patient (weight:NA) experienced the following symptoms/conditions: NA.The patient was prescribed Jurnista (drug dosage: NA), which was initiated on NS. Concurrently used drugs: NA..After starting to take Jurnista the consumer reported adverse symptoms, such as: Asthenia, Bile Duct Cancer, Ileus SpasticThese side effects may potentially be related to Jurnista. The patient was hospitalized.
Jurnista Side Effect Report#6550024-3
Asthenia, Ileus Spastic
This is a report of a male patient (weight: NA) from Korea, Republic Of, suffering from the following health symptoms/conditions: NA, who was treated with Jurnista (dosage: NA, start time: NS), combined with: NA. and developed a serious reaction and side effect(s): Asthenia, Ileus Spastic after the beginning of treatment. This case can indicate the possible existence of increased vulnerability to Jurnista treatment in male patients, resulting in Asthenia side effect. The patient was hospitalized.
Jurnista Side Effect Report#6291193-2
Cardiac Failure, Disorientation
This report suggests a potential Jurnista Cardiac Failure side effect(s) that can have serious consequences. A 40-year-old male patient (weight: NA) from Germany was diagnosed with the following symptoms/conditions: NA and used Jurnista (dosage: NA) starting NS. After starting Jurnista the patient began experiencing various side effects, including: Cardiac Failure, DisorientationAdditional drugs used concurrently: NA. Although Jurnista demonstrated significant improvements in a number of clinically relevant cases, troublesome symptoms, such as Cardiac Failure, may still occur.
Jurnista Side Effect Report#6283284-7
Cardiac Failure, Disorientation
This Cardiac Failure problem was reported by a health professional from Germany. A 40-year-old male patient (weight: NA) was diagnosed with the following symptoms/conditions: NA. On NS this consumer started treatment with Jurnista (dosage: NA). The following drugs were being taken at the same time: NA. When using Jurnista, the patient experienced the following unwanted symptoms/side effects: Cardiac Failure, DisorientationAlthough all drugs are carefully tested before they are licensed for use, they carry side effect risks. Some side effects, such as Cardiac Failure, may become evident only after a product is in use by the general population.
Jurnista Side Effect Report#6201214-0
Accidental Overdose, Dyskinesia
This Accidental Overdose side effect was reported by a physician from Switzerland. A male patient (weight:NA) experienced the following symptoms/conditions: NA.The patient was prescribed Jurnista (drug dosage: NA), which was initiated on NS. Concurrently used drugs: NA..After starting to take Jurnista the consumer reported adverse symptoms, such as: Accidental Overdose, DyskinesiaThese side effects may potentially be related to Jurnista.
Jurnista Side Effect Report#6166070-8
Disorientation, Dyskinesia, Muscle Spasms, Myoclonus, Withdrawal Syndrome
This is a report of a 49-year-old female patient (weight: NA) from Spain, suffering from the following health symptoms/conditions: NA, who was treated with Jurnista (dosage: NA, start time: NS), combined with: NA. and developed a serious reaction and side effect(s): Disorientation, Dyskinesia, Muscle Spasms, Myoclonus, Withdrawal Syndrome after the beginning of treatment. This case can indicate the possible existence of increased vulnerability to Jurnista treatment in female patients, resulting in Disorientation side effect. The patient was hospitalized.
Jurnista Side Effect Report#6165578-9
Disorientation, Dyskinesia, Muscle Spasms, Myoclonus, Withdrawal Syndrome
This report suggests a potential Jurnista Disorientation side effect(s) that can have serious consequences. A 49-year-old female patient (weight: NA) from Spain was diagnosed with the following symptoms/conditions: NA and used Jurnista (dosage: NA) starting NS. After starting Jurnista the patient began experiencing various side effects, including: Disorientation, Dyskinesia, Muscle Spasms, Myoclonus, Withdrawal SyndromeAdditional drugs used concurrently: NA.The patient was hospitalized. Although Jurnista demonstrated significant improvements in a number of clinically relevant cases, troublesome symptoms, such as Disorientation, may still occur.
Jurnista Side Effect Report#6150433-0
Convulsion, Disorientation, Dyskinesia, Withdrawal Syndrome
This Convulsion problem was reported by a physician from Spain. A 49-year-old female patient (weight: NA) was diagnosed with the following symptoms/conditions: NA. On NS this consumer started treatment with Jurnista (dosage: NA). The following drugs were being taken at the same time: NA. When using Jurnista, the patient experienced the following unwanted symptoms/side effects: Convulsion, Disorientation, Dyskinesia, Withdrawal SyndromeThe 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 Convulsion, may become evident only after a product is in use by the general population.
Jurnista Side Effect Report#5623285-2
Accidental Overdose, Respiratory Failure, Restlessness
This Accidental Overdose side effect was reported by a physician from Germany. A 85-year-old male patient (weight:NA) experienced the following symptoms/conditions: pain.The patient was prescribed Jurnista (drug dosage: NA), which was initiated on NS. Concurrently used drugs:
  • Duragesic-100
.After starting to take Jurnista the consumer reported adverse symptoms, such as: Accidental Overdose, Respiratory Failure, RestlessnessThese side effects may potentially be related to Jurnista.
Jurnista Side Effect Report#5423784-2
Depressed Level Of Consciousness, Feeding Tube Complication, Inadequate Analgesia, Oral Intake Reduced, Respiratory Failure, Respiratory Paralysis, Restlessness
This is a report of a 85-year-old male patient (weight: NA) from Germany, suffering from the following health symptoms/conditions: pain, who was treated with Jurnista (dosage: NA, start time: NS), combined with:
  • Duragesic-100
and developed a serious reaction and side effect(s): Depressed Level Of Consciousness, Feeding Tube Complication, Inadequate Analgesia, Oral Intake Reduced, Respiratory Failure, Respiratory Paralysis, Restlessness after the beginning of treatment. This case can indicate the possible existence of increased vulnerability to Jurnista treatment in male patients, resulting in Depressed Level Of Consciousness side effect.



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.

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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.

    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.

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    Discuss Jurnista Side Effects

    Did You Have a Jurnista Side Effect?

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    How Effective is Jurnista for You?

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