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Asunra Side Effects

PatientsVille

Common Asunra Side Effects


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

Death (23)
Pyrexia (6)
Iron Overload (5)
Diarrhoea (4)
Myocardial Infarction (3)
Haematological Malignancy (3)
Blood Creatinine Increased (3)
Albumin Urine Present (3)
Hypertensive Nephropathy (3)
Oedema Peripheral (3)
Somnolence (3)
Swelling Face (3)
Pyuria (3)
Haematemesis (2)
Disease Progression (2)
Post Procedural Complication (2)
Multi-organ Failure (2)
Heart Rate Increased (2)
Pain (2)
Paralysis (2)

➢ 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.

Asunra Side Effects Reported to FDA



Asunra Side Effect Report#9511628
Pain, Movement Disorder, Hypophagia, Gastrointestinal Disorder
This is a report of a 40-year-old female patient (weight: NA) from BD, suffering from the following health symptoms/conditions: thalassaemia, who was treated with Asunra (dosage: 600 Mg, Daily, start time:
Aug 20, 2013), combined with: NA. and developed a serious reaction and side effect(s): Pain, Movement Disorder, Hypophagia, Gastrointestinal Disorder after the beginning of treatment. This case can indicate the possible existence of increased vulnerability to Asunra treatment in female patients, resulting in Pain side effect.
Asunra Side Effect Report#9422183
Pain, Syncope, Dyspnoea
This report suggests a potential Asunra Death side effect(s) that can have serious consequences. A 55-year-old female patient (weight: NA) from IN was diagnosed with the following symptoms/conditions: iron overload and used Asunra (dosage: 400 Mg, Qd) starting
Jun 11, 2012. After starting Asunra the patient began experiencing various side effects, including: Pain, Syncope, DyspnoeaAdditional drugs used concurrently: NA.The patient was hospitalized. Although Asunra demonstrated significant improvements in a number of clinically relevant cases, troublesome symptoms, such as Death, may still occur.
Asunra Side Effect Report#9271129
This Death problem was reported by a physician from PK. A 14-year-old male patient (weight: NA) was diagnosed with the following symptoms/conditions: thalassaemia. On NS this consumer started treatment with Asunra (dosage: 800 Mg, Qd). The following drugs were being taken at the same time: NA. When using Asunra, the patient experienced the following unwanted symptoms/side effects:Although all drugs are carefully tested before they are licensed for use, they carry side effect risks. Some side effects, such as Death, may become evident only after a product is in use by the general population.
Asunra Side Effect Report#9254174
Infection, Heart Rate Increased, Pyrexia
This Infection side effect was reported by a consumer or non-health professional from Country Not Specified. A 8-year-old female patient (weight:NA) experienced the following symptoms/conditions: thalassaemia.The patient was prescribed Asunra (drug dosage: 100 Mg, Daily), which was initiated on NS. Concurrently used drugs: NA..After starting to take Asunra the consumer reported adverse symptoms, such as: Infection, Heart Rate Increased, PyrexiaThese side effects may potentially be related to Asunra.
Asunra Side Effect Report#9244586
Anal Erosion, Anal Fissure, Haemorrhoids, Painful Defaecation, Diarrhoea
This is a report of a 49-year-old male patient (weight: NA) from IN, suffering from the following health symptoms/conditions: myelofibrosis, who was treated with Asunra (dosage: 800 Mg, Per Day, start time: NS), combined with: NA. and developed a serious reaction and side effect(s): Anal Erosion, Anal Fissure, Haemorrhoids, Painful Defaecation, Diarrhoea after the beginning of treatment. This case can indicate the possible existence of increased vulnerability to Asunra treatment in male patients, resulting in Anal Erosion side effect.
Asunra Side Effect Report#9028995
This report suggests a potential Asunra Death side effect(s) that can have serious consequences. A 33-year-old male patient (weight: NA) from IN was diagnosed with the following symptoms/conditions: thalassaemia and used Asunra (dosage: 400 Mg X 3) starting
Jun 02, 2012. After starting Asunra the patient began experiencing various side effects, including:Additional drugs used concurrently: NA. Although Asunra demonstrated significant improvements in a number of clinically relevant cases, troublesome symptoms, such as Death, may still occur.
Asunra Side Effect Report#8973954
Dengue Fever
This Dengue Fever problem was reported by a physician from IN. A 65-year-old male patient (weight: NA) was diagnosed with the following symptoms/conditions: thalassaemia. On
Jan 24, 2012 this consumer started treatment with Asunra (dosage: 1600 Mg, Qd). The following drugs were being taken at the same time: NA. When using Asunra, the patient experienced the following unwanted symptoms/side effects: Dengue FeverThe 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 Dengue Fever, may become evident only after a product is in use by the general population.
Asunra Side Effect Report#8138600-8
This Death side effect was reported by a consumer or non-health professional from Bangladesh. A 24-year-old female patient (weight:NA) experienced the following symptoms/conditions: thalassaemia.The patient was prescribed Asunra (drug dosage: Unk Ukn, Unk), which was initiated on NS. Concurrently used drugs: NA..After starting to take Asunra the consumer reported adverse symptoms, such as: These side effects may potentially be related to Asunra.
Asunra Side Effect Report#7561910-X
Paralysis, Cardiac Disorder
This is a report of a 12-year-old female patient (weight: NA) from India, suffering from the following health symptoms/conditions: iron overload, who was treated with Asunra (dosage: 400 Mg, start time:
Jan 01, 2009), combined with: NA. and developed a serious reaction and side effect(s): Paralysis, Cardiac Disorder after the beginning of treatment. This case can indicate the possible existence of increased vulnerability to Asunra treatment in female patients, resulting in Death side effect. The patient was hospitalized.
Asunra Side Effect Report#7437091-X
This report suggests a potential Asunra Death side effect(s) that can have serious consequences. A 4-year-old female patient (weight: NA) from India was diagnosed with the following symptoms/conditions: NA and used Asunra (dosage: 300mg (3 Tablets Of 100mg).) starting NS. After starting Asunra the patient began experiencing various side effects, including:Additional drugs used concurrently: NA. Although Asunra demonstrated significant improvements in a number of clinically relevant cases, troublesome symptoms, such as Death, may still occur.
Asunra Side Effect Report#7431804-9
Cerebral Haemorrhage
This Cerebral Haemorrhage problem was reported by a consumer or non-health professional from India. A 19-year-old male patient (weight: NA) was diagnosed with the following symptoms/conditions: NA. On NS this consumer started treatment with Asunra (dosage: 400 Mg, Unk). The following drugs were being taken at the same time: NA. When using Asunra, the patient experienced the following unwanted symptoms/side effects: Cerebral HaemorrhageAlthough all drugs are carefully tested before they are licensed for use, they carry side effect risks. Some side effects, such as Cerebral Haemorrhage, may become evident only after a product is in use by the general population.
Asunra Side Effect Report#7354012-9
Transplant Failure, Haemoglobin Decreased, Platelet Count Decreased
This Transplant Failure side effect was reported by a consumer or non-health professional from India. A 75-year-old female patient (weight:NA) experienced the following symptoms/conditions: NA.The patient was prescribed Asunra (drug dosage: 400 Mg, Daily), which was initiated on NS. Concurrently used drugs: NA..After starting to take Asunra the consumer reported adverse symptoms, such as: Transplant Failure, Haemoglobin Decreased, Platelet Count DecreasedThese side effects may potentially be related to Asunra.
Asunra Side Effect Report#7291608-7
Lung Infection
This is a report of a 14-year-old male patient (weight: NA) from India, suffering from the following health symptoms/conditions: NA, who was treated with Asunra (dosage: 400 Mg, start time: NS), combined with: NA. and developed a serious reaction and side effect(s): Lung Infection after the beginning of treatment. This case can indicate the possible existence of increased vulnerability to Asunra treatment in male patients, resulting in Lung Infection side effect.
Asunra Side Effect Report#7279098-1
This report suggests a potential Asunra Death side effect(s) that can have serious consequences. A 25-year-old male patient (weight: NA) from India was diagnosed with the following symptoms/conditions: NA and used Asunra (dosage: 100 Mg, Unk) starting NS. After starting Asunra the patient began experiencing various side effects, including:Additional drugs used concurrently: NA. Although Asunra demonstrated significant improvements in a number of clinically relevant cases, troublesome symptoms, such as Death, may still occur.
Asunra Side Effect Report#7265158-8
Chest Pain, Haematemesis
This Chest Pain problem was reported by a physician from India. A 22-year-old male patient (weight: NA) was diagnosed with the following symptoms/conditions: NA. On NS this consumer started treatment with Asunra (dosage: 400 Mg, Unk). The following drugs were being taken at the same time: NA. When using Asunra, the patient experienced the following unwanted symptoms/side effects: Chest Pain, HaematemesisAlthough all drugs are carefully tested before they are licensed for use, they carry side effect risks. Some side effects, such as Chest Pain, may become evident only after a product is in use by the general population.
Asunra Side Effect Report#7243682-1
Haematemesis, Paralysis
This Haematemesis side effect was reported by a consumer or non-health professional from India. A 13-year-old female patient (weight:NA) experienced the following symptoms/conditions: NA.The patient was prescribed Asunra (drug dosage: NA), which was initiated on NS. Concurrently used drugs: NA..After starting to take Asunra the consumer reported adverse symptoms, such as: Haematemesis, ParalysisThese side effects may potentially be related to Asunra.
Asunra Side Effect Report#7214644-5
Pyuria, Hypertensive Nephropathy, Swelling Face, Oedema Peripheral, Blood Creatinine Increased, Albumin Urine Present
This is a report of a 19-year-old female patient (weight: NA) from India, suffering from the following health symptoms/conditions: iron overload,thalassaemia beta, who was treated with Asunra (dosage: 25 Mg/kg/day, start time:
Sep 09, 2008), combined with: NA. and developed a serious reaction and side effect(s): Pyuria, Hypertensive Nephropathy, Swelling Face, Oedema Peripheral, Blood Creatinine Increased, Albumin Urine Present after the beginning of treatment. This case can indicate the possible existence of increased vulnerability to Asunra treatment in female patients, resulting in Pyuria side effect.
Asunra Side Effect Report#7150474-0
This report suggests a potential Asunra Death side effect(s) that can have serious consequences. A 75-year-old female patient (weight: NA) from India was diagnosed with the following symptoms/conditions: NA and used Asunra (dosage: 400 Mg, Unk) starting NS. After starting Asunra the patient began experiencing various side effects, including:Additional drugs used concurrently: NA. Although Asunra demonstrated significant improvements in a number of clinically relevant cases, troublesome symptoms, such as Death, may still occur.
Asunra Side Effect Report#7145051-1
Albumin Urine Present, Blood Creatinine Increased, Hypertensive Nephropathy, Oedema Peripheral, Pyuria, Swelling Face
This Albumin Urine Present problem was reported by a physician from India. A 19-year-old female patient (weight: NA) was diagnosed with the following symptoms/conditions: thalassaemia beta,iron overload. On
Sep 09, 2008 this consumer started treatment with Asunra (dosage: 1200 Mg, Unk). The following drugs were being taken at the same time: NA. When using Asunra, the patient experienced the following unwanted symptoms/side effects: Albumin Urine Present, Blood Creatinine Increased, Hypertensive Nephropathy, Oedema Peripheral, Pyuria, Swelling FaceAlthough all drugs are carefully tested before they are licensed for use, they carry side effect risks. Some side effects, such as Albumin Urine Present, may become evident only after a product is in use by the general population.
Asunra Side Effect Report#7132297-1
Hepatic Infection
This Hepatic Infection side effect was reported by a consumer or non-health professional from India. A 73-year-old male patient (weight:NA) experienced the following symptoms/conditions: NA.The patient was prescribed Asunra (drug dosage: 400 Mg, Unk), which was initiated on NS. Concurrently used drugs: NA..After starting to take Asunra the consumer reported adverse symptoms, such as: Hepatic InfectionThese side effects may potentially be related to Asunra.
Asunra Side Effect Report#7068938-7
This is a report of a 8-year-old female patient (weight: NA) from India, suffering from the following health symptoms/conditions: NA, who was treated with Asunra (dosage: 1 Tablet Of 400 Mg And 1 Tablet Of 100 Mg), start time:
May 01, 2010), combined with: NA. and developed a serious reaction and side effect(s): after the beginning of treatment. This case can indicate the possible existence of increased vulnerability to Asunra treatment in female patients, resulting in Death side effect.
Asunra Side Effect Report#7055581-9
Myelodysplastic Syndrome
This report suggests a potential Asunra Myelodysplastic Syndrome side effect(s) that can have serious consequences. A 53-year-old female patient (weight: NA) from India was diagnosed with the following symptoms/conditions: NA and used Asunra (dosage: 400 Mg, 2 Tablets) starting NS. After starting Asunra the patient began experiencing various side effects, including: Myelodysplastic SyndromeAdditional drugs used concurrently: NA. Although Asunra demonstrated significant improvements in a number of clinically relevant cases, troublesome symptoms, such as Myelodysplastic Syndrome, may still occur.
Asunra Side Effect Report#6914111-X
This Death problem was reported by a consumer or non-health professional from India. A 15-year-old male patient (weight: NA) was diagnosed with the following symptoms/conditions: NA. On NS this consumer started treatment with Asunra (dosage: 2 Tab Of 400mg). The following drugs were being taken at the same time: NA. When using Asunra, the patient experienced the following unwanted symptoms/side effects:Although all drugs are carefully tested before they are licensed for use, they carry side effect risks. Some side effects, such as Death, may become evident only after a product is in use by the general population.
Asunra Side Effect Report#6907968-X
Cerebral Haemorrhage, Diarrhoea, Haematological Malignancy, Pyrexia
This Cerebral Haemorrhage side effect was reported by a consumer or non-health professional from India. A 58-year-old male patient (weight:NA) experienced the following symptoms/conditions: NA.The patient was prescribed Asunra (drug dosage: 400 Mg, Bid), which was initiated on NS. Concurrently used drugs: NA..After starting to take Asunra the consumer reported adverse symptoms, such as: Cerebral Haemorrhage, Diarrhoea, Haematological Malignancy, PyrexiaThese side effects may potentially be related to Asunra. The patient was hospitalized.
Asunra Side Effect Report#6895585-X
Pharyngitis
This is a report of a 11-year-old male patient (weight: NA) from India, suffering from the following health symptoms/conditions: NA, who was treated with Asunra (dosage: 400 Mg, One Tablet, start time: NS), combined with: NA. and developed a serious reaction and side effect(s): Pharyngitis after the beginning of treatment. This case can indicate the possible existence of increased vulnerability to Asunra treatment in male patients, resulting in Pharyngitis side effect.


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The appearance of Asunra 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.


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.

    Asunra 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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    Asunra Safety Alerts, Active Ingredients, Usage Information

    More About Asunra

    Side Effects reported to FDA: 66

    Asunra safety alerts: No

    Reported deaths: 63

    Reported hospitalizations: 10

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