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Eskazole Side Effects

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Common Eskazole Side Effects


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

White Blood Cell Count Decreased (6)
Hepatic Enzyme Increased (5)
Hip Dysplasia (4)
Alopecia (4)
Gamma-glutamyltransferase Increased (3)
Aspartate Aminotransferase Increased (3)
Arrhythmia (3)
Alanine Aminotransferase Increased (3)
Hepatitis (3)
Leukopenia (3)
Transaminases Increased (3)
Pancytopenia (3)
Palpitations (3)
Osteoarthritis (3)
Liver Abscess (2)
Hepatitis Toxic (2)
Liver Disorder (2)
Supraventricular Tachycardia (2)
Pruritus (2)
Neutrophil Count Decreased (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.

Eskazole Side Effects Reported to FDA



Eskazole Side Effect Report#7586412-6
Blood Immunoglobulin E Increased, Computerised Tomogram Thorax Abnormal, Eosinophil Count Increased, Rash, Pruritus, Liver Disorder, Malaise, Hepatic Enzyme Increased
This is a report of a 36-year-old male patient (weight: NA) from Japan, suffering from the following health symptoms/conditions: toxocariasis, who was treated with Eskazole (dosage: 1000mg Per Day, start time:
Sep 14, 2009), combined with: NA. and developed a serious reaction and side effect(s): Blood Immunoglobulin E Increased, Computerised Tomogram Thorax Abnormal, Eosinophil Count Increased, Rash, Pruritus, Liver Disorder, Malaise, Hepatic Enzyme Increased after the beginning of treatment. This case can indicate the possible existence of increased vulnerability to Eskazole treatment in male patients, resulting in Blood Immunoglobulin E Increased side effect.
Eskazole Side Effect Report#7133056-6
Disseminated Intravascular Coagulation, Leukopenia, Liver Abscess, Multi-organ Failure, Pyrexia, White Blood Cell Count Decreased
This report suggests a potential Eskazole Disseminated Intravascular Coagulation side effect(s) that can have serious consequences. A 73-year-old male patient (weight: NA) from Japan was diagnosed with the following symptoms/conditions: NA and used Eskazole (dosage: 600mg Per Day) starting NS. After starting Eskazole the patient began experiencing various side effects, including: Disseminated Intravascular Coagulation, Leukopenia, Liver Abscess, Multi-organ Failure, Pyrexia, White Blood Cell Count DecreasedAdditional drugs used concurrently: NA.The patient was hospitalized. Although Eskazole demonstrated significant improvements in a number of clinically relevant cases, troublesome symptoms, such as Disseminated Intravascular Coagulation, may still occur.
Eskazole Side Effect Report#6740225-3
Transaminases Increased
This Transaminases Increased problem was reported by a consumer or non-health professional from Japan. A 42-year-old female patient (weight: NA) was diagnosed with the following symptoms/conditions: toxocariasis. On NS this consumer started treatment with Eskazole (dosage: NA). The following drugs were being taken at the same time: NA. When using Eskazole, the patient experienced the following unwanted symptoms/side effects: Transaminases IncreasedAlthough all drugs are carefully tested before they are licensed for use, they carry side effect risks. Some side effects, such as Transaminases Increased, may become evident only after a product is in use by the general population.
Eskazole Side Effect Report#6572187-6
Polyneuropathy
This Death side effect was reported by a health professional from Germany. A 60-year-old male patient (weight:NA) experienced the following symptoms/conditions: NA.The patient was prescribed Eskazole (drug dosage: NA), which was initiated on NS. Concurrently used drugs: NA..After starting to take Eskazole the consumer reported adverse symptoms, such as: PolyneuropathyThese side effects may potentially be related to Eskazole.
Eskazole Side Effect Report#6556420-2
Acute Hepatic Failure, Alopecia, Bile Duct Obstruction, Ultrasound Scan Abnormal
This is a report of a female patient (weight: NA) from Spain, suffering from the following health symptoms/conditions: hepatic echinococciasis, who was treated with Eskazole (dosage: NA, start time:
Aug 20, 2009), combined with: NA. and developed a serious reaction and side effect(s): Acute Hepatic Failure, Alopecia, Bile Duct Obstruction, Ultrasound Scan Abnormal after the beginning of treatment. This case can indicate the possible existence of increased vulnerability to Eskazole treatment in female patients, resulting in Acute Hepatic Failure side effect.
Eskazole Side Effect Report#6405674-1
Acute Hepatic Failure, Alopecia
This report suggests a potential Eskazole Acute Hepatic Failure side effect(s) that can have serious consequences. A 58-year-old female patient (weight: NA) from Spain was diagnosed with the following symptoms/conditions: NA and used Eskazole (dosage: NA) starting
Aug 20, 2009. After starting Eskazole the patient began experiencing various side effects, including: Acute Hepatic Failure, AlopeciaAdditional drugs used concurrently: NA. Although Eskazole demonstrated significant improvements in a number of clinically relevant cases, troublesome symptoms, such as Acute Hepatic Failure, may still occur.
Eskazole Side Effect Report#6155738-5
Pancytopenia
This Pancytopenia problem was reported by a consumer or non-health professional from Spain. A 78-year-old female patient (weight: NA) was diagnosed with the following symptoms/conditions: NA. On
Mar 02, 2009 this consumer started treatment with Eskazole (dosage: NA). The following drugs were being taken at the same time: NA. When using Eskazole, the patient experienced the following unwanted symptoms/side effects: PancytopeniaThe 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 Pancytopenia, may become evident only after a product is in use by the general population.
Eskazole Side Effect Report#6051566-X
Erythema Multiforme, Leukopenia, Neutropenia, Toxic Skin Eruption
This Erythema Multiforme side effect was reported by a consumer or non-health professional from France. A 71-year-old male patient (weight:NA) experienced the following symptoms/conditions: pulmonary echinococciasis.The patient was prescribed Eskazole (drug dosage: 100mg Twice Per Day), which was initiated on
Jun 01, 2008. Concurrently used drugs: NA..After starting to take Eskazole the consumer reported adverse symptoms, such as: Erythema Multiforme, Leukopenia, Neutropenia, Toxic Skin EruptionThese side effects may potentially be related to Eskazole.
Eskazole Side Effect Report#6021396-3
Liver Abscess, White Blood Cell Count Decreased
This is a report of a 73-year-old male patient (weight: NA) from Japan, suffering from the following health symptoms/conditions: NA, who was treated with Eskazole (dosage: NA, start time: NS), combined with: NA. and developed a serious reaction and side effect(s): Liver Abscess, White Blood Cell Count Decreased after the beginning of treatment. This case can indicate the possible existence of increased vulnerability to Eskazole treatment in male patients, resulting in Liver Abscess side effect.
Eskazole Side Effect Report#5987029-7
Alanine Aminotransferase Increased, Aspartate Aminotransferase Increased, Liver Disorder
This report suggests a potential Eskazole Alanine Aminotransferase Increased side effect(s) that can have serious consequences. A 42-year-old female patient (weight: NA) from Japan was diagnosed with the following symptoms/conditions: toxocariasis and used Eskazole (dosage: 200mg Three Times Per Day) starting
Sep 06, 2008. After starting Eskazole the patient began experiencing various side effects, including: Alanine Aminotransferase Increased, Aspartate Aminotransferase Increased, Liver DisorderAdditional drugs used concurrently: NA. Although Eskazole demonstrated significant improvements in a number of clinically relevant cases, troublesome symptoms, such as Alanine Aminotransferase Increased, may still occur.
Eskazole Side Effect Report#5891016-7
Bone Marrow Failure, Granulocytopenia, Leukopenia
This Bone Marrow Failure problem was reported by a consumer or non-health professional from Netherlands. A 61-year-old female patient (weight: NA) was diagnosed with the following symptoms/conditions: echinococciasis. On
May 14, 2008 this consumer started treatment with Eskazole (dosage: 400mg Twice Per Day). The following drugs were being taken at the same time:
  • Alendronate Sodium (70mg Weekly)
  • Pantozol (40mg Per Day)
  • Acetaminophen (500mg Four Times Per Day)
  • Spironolactone (200mg Per Day)
  • Temazepam (10mg Per Day)
When using Eskazole, the patient experienced the following unwanted symptoms/side effects: Bone Marrow Failure, Granulocytopenia, LeukopeniaThe 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 Bone Marrow Failure, may become evident only after a product is in use by the general population.
Eskazole Side Effect Report#5859577-1
Hepatic Enzyme Increased, Hepatitis
This Hepatic Enzyme Increased side effect was reported by a consumer or non-health professional from France. A 55-year-old male patient (weight:NA) experienced the following symptoms/conditions: NA.The patient was prescribed Eskazole (drug dosage: NA), which was initiated on
Dec 18, 2006. Concurrently used drugs:
  • Parkinane
  • Trivastal
  • Prozac
  • Selegiline Hcl
.After starting to take Eskazole the consumer reported adverse symptoms, such as: Hepatic Enzyme Increased, HepatitisThese side effects may potentially be related to Eskazole.
Eskazole Side Effect Report#5856284-6
Endometrial Cancer, Gamma-glutamyltransferase Increased, Transaminases Increased
This is a report of a 72-year-old female patient (weight: NA) from France, suffering from the following health symptoms/conditions: NA, who was treated with Eskazole (dosage: NA, start time:
Mar 18, 2008), combined with:
  • Hyperium
  • Furosemide
  • Iskedyl
  • Advil Liqui-gels
  • Daflon
and developed a serious reaction and side effect(s): Endometrial Cancer, Gamma-glutamyltransferase Increased, Transaminases Increased after the beginning of treatment. This case can indicate the possible existence of increased vulnerability to Eskazole treatment in female patients, resulting in Endometrial Cancer side effect.
Eskazole Side Effect Report#5856283-4
Asthenia, Gamma-glutamyltransferase Increased, Hepatitis, Transaminases Increased
This report suggests a potential Eskazole Asthenia side effect(s) that can have serious consequences. A 73-year-old male patient (weight: NA) from France was diagnosed with the following symptoms/conditions: NA and used Eskazole (dosage: NA) starting
Nov 26, 2007. After starting Eskazole the patient began experiencing various side effects, including: Asthenia, Gamma-glutamyltransferase Increased, Hepatitis, Transaminases IncreasedAdditional drugs used concurrently:
  • Irbesartan
  • Avandia
  • Pravastatin
Although Eskazole demonstrated significant improvements in a number of clinically relevant cases, troublesome symptoms, such as Asthenia, may still occur.
Eskazole Side Effect Report#5781955-X
Histiocytosis Haematophagic
This Histiocytosis Haematophagic problem was reported by a physician from Japan. A 87-year-old female patient (weight: NA) was diagnosed with the following symptoms/conditions: hepatic echinococciasis. On NS this consumer started treatment with Eskazole (dosage: 200mg Three Times Per Day). The following drugs were being taken at the same time: NA. When using Eskazole, the patient experienced the following unwanted symptoms/side effects: Histiocytosis HaematophagicThe 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 Histiocytosis Haematophagic, may become evident only after a product is in use by the general population.
Eskazole Side Effect Report#5781954-8
Alopecia, Anaemia, Neutrophil Count Decreased
This Alopecia side effect was reported by a physician from Japan. A 30-year-old male patient (weight:NA) experienced the following symptoms/conditions: NA.The patient was prescribed Eskazole (drug dosage: 200mg Three Times Per Day), which was initiated on NS. Concurrently used drugs: NA..After starting to take Eskazole the consumer reported adverse symptoms, such as: Alopecia, Anaemia, Neutrophil Count DecreasedThese side effects may potentially be related to Eskazole. The patient was hospitalized.
Eskazole Side Effect Report#5781953-6
Neutrophil Count Decreased, Pneumonia, Sepsis
This is a report of a 62-year-old male patient (weight: NA) from Japan, suffering from the following health symptoms/conditions: hepatic echinococciasis, who was treated with Eskazole (dosage: 200mg Three Times Per Day, start time: NS), combined with: NA. and developed a serious reaction and side effect(s): Neutrophil Count Decreased, Pneumonia, Sepsis after the beginning of treatment. This case can indicate the possible existence of increased vulnerability to Eskazole treatment in male patients, resulting in Neutrophil Count Decreased side effect. The patient was hospitalized.
Eskazole Side Effect Report#5781921-4
Arrhythmia, Palpitations, Supraventricular Tachycardia, White Blood Cell Count Decreased
This report suggests a potential Eskazole Arrhythmia side effect(s) that can have serious consequences. A 70-year-old female patient (weight: NA) from Japan was diagnosed with the following symptoms/conditions: hepatic echinococciasis,gastritis and used Eskazole (dosage: 200mg Three Times Per Day) starting
Feb 06, 2008. After starting Eskazole the patient began experiencing various side effects, including: Arrhythmia, Palpitations, Supraventricular Tachycardia, White Blood Cell Count DecreasedAdditional drugs used concurrently:
  • Famotidine (20mg Twice Per Day)
  • Biofermin R (1g Twice Per Day)
  • Kaytwo (5mg Twice Per Day)
  • Spelear (200mg Twice Per Day)
  • Ferromia (50mg Per Day)
The patient was hospitalized. Although Eskazole demonstrated significant improvements in a number of clinically relevant cases, troublesome symptoms, such as Arrhythmia, may still occur.
Eskazole Side Effect Report#5759798-2
Abortion Missed, Excoriation
This Abortion Missed problem was reported by a physician from Germany. A 36-year-old female patient (weight: NA) was diagnosed with the following symptoms/conditions: infection parasitic. On
Apr 28, 2008 this consumer started treatment with Eskazole (dosage: 400mg Per Day). The following drugs were being taken at the same time: NA. When using Eskazole, the patient experienced the following unwanted symptoms/side effects: Abortion Missed, ExcoriationAlthough all drugs are carefully tested before they are licensed for use, they carry side effect risks. Some side effects, such as Abortion Missed, may become evident only after a product is in use by the general population.
Eskazole Side Effect Report#5718001-X
Arrhythmia, Cardiac Disorder, Palpitations, Supraventricular Tachycardia, White Blood Cell Count Decreased
This Arrhythmia side effect was reported by a physician from Japan. A 70-year-old female patient (weight:NA) experienced the following symptoms/conditions: hepatic echinococciasis,gastritis,diarrhoea,haemorrhage prophylaxis,productive cough,anaemia.The patient was prescribed Eskazole (drug dosage: 200mg Three Times Per Day), which was initiated on
Feb 06, 2008. Concurrently used drugs:
  • Gaster D (20mg Twice Per Day)
  • Biofermin R (1g Twice Per Day)
  • Kaytwo (5mg Twice Per Day)
  • Spelear (200mg Twice Per Day)
  • Ferrous Sulfate Tab (50mg Per Day)
.After starting to take Eskazole the consumer reported adverse symptoms, such as: Arrhythmia, Cardiac Disorder, Palpitations, Supraventricular Tachycardia, White Blood Cell Count DecreasedThese side effects may potentially be related to Eskazole. The patient was hospitalized.
Eskazole Side Effect Report#5702762-X
Arrhythmia, Palpitations, Tachycardia, White Blood Cell Count Decreased
This is a report of a 70-year-old female patient (weight: NA) from Japan, suffering from the following health symptoms/conditions: hepatic echinococciasis,gastritis, who was treated with Eskazole (dosage: 200mg Three Times Per Day, start time:
Feb 06, 2008), combined with:
  • Gaster D (20mg Twice Per Day)
  • Biofermin R (1g Twice Per Day)
  • Kaytwo (5mg Twice Per Day)
  • Spelear (200mg Twice Per Day)
  • Ferromia (50mg Per Day)
and developed a serious reaction and side effect(s): Arrhythmia, Palpitations, Tachycardia, White Blood Cell Count Decreased after the beginning of treatment. This case can indicate the possible existence of increased vulnerability to Eskazole treatment in female patients, resulting in Arrhythmia side effect. The patient was hospitalized.
Eskazole Side Effect Report#5670913-1
Alopecia, Pancytopenia, Red Blood Cell Count Decreased, White Blood Cell Count Decreased
This report suggests a potential Eskazole Alopecia side effect(s) that can have serious consequences. A 73-year-old male patient (weight: NA) from Japan was diagnosed with the following symptoms/conditions: echinococciasis and used Eskazole (dosage: 200mg Three Times Per Day) starting
Jan 24, 2008. After starting Eskazole the patient began experiencing various side effects, including: Alopecia, Pancytopenia, Red Blood Cell Count Decreased, White Blood Cell Count DecreasedAdditional drugs used concurrently:
  • Glycyron
  • Urso 250 (300mg Per Day)
  • Gaslon N (4mg Per Day)
  • Harnal (.2mg Per Day)
The patient was hospitalized. Although Eskazole demonstrated significant improvements in a number of clinically relevant cases, troublesome symptoms, such as Alopecia, may still occur.
Eskazole Side Effect Report#5149325-5
Aspartate Aminotransferase Increased, Hepatic Enzyme Increased, Hepatitis
This Aspartate Aminotransferase Increased problem was reported by a physician from Germany. A 28-year-old female patient (weight: NA) was diagnosed with the following symptoms/conditions: echinococciasis. On
Nov 29, 2005 this consumer started treatment with Eskazole (dosage: 400mg Twice Per Day). The following drugs were being taken at the same time: NA. When using Eskazole, the patient experienced the following unwanted symptoms/side effects: Aspartate Aminotransferase Increased, Hepatic Enzyme Increased, HepatitisAlthough all drugs are carefully tested before they are licensed for use, they carry side effect risks. Some side effects, such as Aspartate Aminotransferase Increased, may become evident only after a product is in use by the general population.
Eskazole Side Effect Report#5022296-8
Hepatitis Toxic
This Hepatitis Toxic side effect was reported by a consumer or non-health professional from France. A 30-year-old male patient (weight:NA) experienced the following symptoms/conditions: hepatic echinococciasis.The patient was prescribed Eskazole (drug dosage: 200mg Four Times Per Day), which was initiated on
Dec 06, 2005. Concurrently used drugs: NA..After starting to take Eskazole the consumer reported adverse symptoms, such as: Hepatitis ToxicThese side effects may potentially be related to Eskazole. The patient was hospitalized.
Eskazole Side Effect Report#4922604-X
Hip Dysplasia, Osteoarthritis
This is a report of a 36-year-old male patient (weight: NA) from Germany, suffering from the following health symptoms/conditions: echinococciasis, who was treated with Eskazole (dosage: 400mg Twice Per Day, start time:
Apr 19, 2002), combined with:
  • Diclac
and developed a serious reaction and side effect(s): Hip Dysplasia, Osteoarthritis after the beginning of treatment. This case can indicate the possible existence of increased vulnerability to Eskazole treatment in male patients, resulting in Hip Dysplasia side effect.


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The appearance of Eskazole 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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Why Your Notes are Important

Your notes could be helpful in several ways:

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    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.

    Eskazole 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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    Side Effects reported to FDA: 32

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    Reported deaths: 4

    Reported hospitalizations: 13

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