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Aleviatin Side Effects

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Common Aleviatin Side Effects


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

Epilepsy (3)
Agranulocytosis (3)
C-reactive Protein Increased (3)
Bicytopenia (3)
Anaemia (3)
Depressed Level Of Consciousness (2)
Aspartate Aminotransferase Increased (2)
Decreased Activity (2)
Gamma-glutamyltransferase Increased (2)
Hypothermia (2)
Urinary Tract Infection (2)
White Blood Cell Count Increased (2)
Platelet Count Decreased (2)
Hypospadias (1)
Leukopenia (1)
Hepatic Function Abnormal (1)
Erythema (1)
Eating Disorder (1)
Fibrin D Dimer Increased (1)
Fibrin Degradation Products Increased (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.

Aleviatin Side Effects Reported to FDA



Aleviatin Side Effect Report#8158660-8
Convulsion, Panic Disorder
This is a report of a 59-year-old female patient (weight: NA) from Japan, suffering from the following health symptoms/conditions: NA, who was treated with Aleviatin (phenytoin) (dosage: NA, start time:
Dec 28, 2011), combined with:
  • Lamictal
  • Lansoprazole (15 Mg (15 Mg, 1 In 1 D) Per Oral)
and developed a serious reaction and side effect(s): Convulsion, Panic Disorder after the beginning of treatment. This case can indicate the possible existence of increased vulnerability to Aleviatin (phenytoin) treatment in female patients, resulting in Convulsion side effect. The patient was hospitalized.
Aleviatin Side Effect Report#5842300-4
Agranulocytosis, Anaemia, Bicytopenia
This report suggests a potential Aleviatin Agranulocytosis side effect(s) that can have serious consequences. A male patient (weight: NA) from Japan was diagnosed with the following symptoms/conditions: epilepsy,gastritis,depression,hypertension,thrombosis prophylaxis,carotid artery stenosis,cerebral infarction,insomnia,benign prostatic hyperplasia and used Aleviatin (dosage: NA) starting
Jan 01, 2005. After starting Aleviatin the patient began experiencing various side effects, including: Agranulocytosis, Anaemia, BicytopeniaAdditional drugs used concurrently:
  • Famotidine
  • Luvox
  • Diovan
  • Plavix
  • Plavix
  • Plavix
  • Myslee
  • Avishot
The patient was hospitalized. Although Aleviatin demonstrated significant improvements in a number of clinically relevant cases, troublesome symptoms, such as Agranulocytosis, may still occur.
Aleviatin Side Effect Report#5832188-X
Agranulocytosis, Anaemia, Bicytopenia
This Agranulocytosis problem was reported by a pharmacist from Japan. A male patient (weight: NA) was diagnosed with the following symptoms/conditions: epilepsy,gastritis,depression,hypertension,thrombosis prophylaxis,carotid artery stenosis,cerebral infarction,insomnia,benign prostatic hyperplasia. On
Jan 01, 2007 this consumer started treatment with Aleviatin (dosage: NA). The following drugs were being taken at the same time:
  • Famotidine
  • Luvox
  • Diovan
  • Plavix
  • Plavix
  • Plavix
  • Myslee
  • Avishot
When using Aleviatin, the patient experienced the following unwanted symptoms/side effects: Agranulocytosis, Anaemia, BicytopeniaThe 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 Agranulocytosis, may become evident only after a product is in use by the general population.
Aleviatin Side Effect Report#5807603-8
Agranulocytosis, Anaemia, Bicytopenia
This Agranulocytosis side effect was reported by a pharmacist from Japan. A female patient (weight:NA) experienced the following symptoms/conditions: epilepsy,gastritis,neurogenic bladder,hypertension,depression,benign prostatic hyperplasia,schizophrenia.The patient was prescribed Aleviatin (drug dosage: NA), which was initiated on
May 07, 2008. Concurrently used drugs:
  • Gaster
  • Ubretid
  • Fluitran
  • Luvox
  • Avishot
  • Risperdal
  • Adalat
  • Aspirin
.After starting to take Aleviatin the consumer reported adverse symptoms, such as: Agranulocytosis, Anaemia, BicytopeniaThese side effects may potentially be related to Aleviatin. The patient was hospitalized.
Aleviatin Side Effect Report#5690960-3
Leukopenia, Neutropenia
This is a report of a 55-year-old female patient (weight: NA) from Japan, suffering from the following health symptoms/conditions: epilepsy,colon cancer, who was treated with Aleviatin (dosage: NA, start time:
Apr 14, 2007), combined with:
  • Elplat (100 Mg/body=69 Mg/m2)
  • Depakene
  • Leucovorin Calcium (235 Mg/body=162.1 Mg/m2)
  • Fluorouracil (420 Mg/body=289.7 Mg/m2 In Bolus Then 2800 Mg/body=1931 Mg/m2 As Infusion Unk)
  • Phenobal
and developed a serious reaction and side effect(s): Leukopenia, Neutropenia after the beginning of treatment. This case can indicate the possible existence of increased vulnerability to Aleviatin treatment in female patients, resulting in Leukopenia side effect.
Aleviatin Side Effect Report#5618926-X
Liver Disorder
This report suggests a potential Aleviatin Liver Disorder side effect(s) that can have serious consequences. A 57-year-old female patient (weight: NA) from Japan was diagnosed with the following symptoms/conditions: NA and used Aleviatin (dosage: Unk) starting
May 01, 2006. After starting Aleviatin the patient began experiencing various side effects, including: Liver DisorderAdditional drugs used concurrently:
  • Myslee (10 Mg)
Although Aleviatin demonstrated significant improvements in a number of clinically relevant cases, troublesome symptoms, such as Liver Disorder, may still occur.
Aleviatin Side Effect Report#5393282-3
Dermatitis Exfoliative, Diarrhoea, Disseminated Intravascular Coagulation, Epilepsy, Erythema, Sepsis, Stevens-johnson Syndrome
This Dermatitis Exfoliative problem was reported by a physician from Japan. A 86-year-old female patient (weight: NA) was diagnosed with the following symptoms/conditions: NA. On NS this consumer started treatment with Aleviatin (dosage: NA). The following drugs were being taken at the same time:
  • Myslee
  • Candesartan Cilexetil
  • Trichlormethiazide
  • Depakene
  • Tegretol
When using Aleviatin, the patient experienced the following unwanted symptoms/side effects: Dermatitis Exfoliative, Diarrhoea, Disseminated Intravascular Coagulation, Epilepsy, Erythema, Sepsis, Stevens-johnson SyndromeAlthough all drugs are carefully tested before they are licensed for use, they carry side effect risks. Some side effects, such as Dermatitis Exfoliative, may become evident only after a product is in use by the general population.
Aleviatin Side Effect Report#5378870-2
Hepatic Function Abnormal
This Hepatic Function Abnormal side effect was reported by a health professional from Japan. A male patient (weight:NA) experienced the following symptoms/conditions: NA.The patient was prescribed Aleviatin (drug dosage: 200 Mg), which was initiated on
Dec 26, 2006. Concurrently used drugs:
  • Magmitt (1800 Mg)
  • Gaster D (20 Mg)
  • Clopidogrel (75 Mg)
.After starting to take Aleviatin the consumer reported adverse symptoms, such as: Hepatic Function AbnormalThese side effects may potentially be related to Aleviatin. The patient was hospitalized.
Aleviatin Side Effect Report#5262693-9
Depressed Level Of Consciousness
This is a report of a 16-year-old female patient (weight: NA) from Japan, suffering from the following health symptoms/conditions: cerebral palsy, who was treated with Aleviatin (dosage: NA, start time:
Feb 11, 2007), combined with: NA. and developed a serious reaction and side effect(s): Depressed Level Of Consciousness after the beginning of treatment. This case can indicate the possible existence of increased vulnerability to Aleviatin treatment in female patients, resulting in Depressed Level Of Consciousness side effect. The patient was hospitalized.
Aleviatin Side Effect Report#5142020-8
Hypospadias
This report suggests a potential Aleviatin Hypospadias side effect(s) that can have serious consequences. A male patient (weight: NA) from Japan was diagnosed with the following symptoms/conditions: NA and used Aleviatin (dosage: Maternal Dose 500 Mg/day) starting NS. After starting Aleviatin the patient began experiencing various side effects, including: HypospadiasAdditional drugs used concurrently:
  • Diamox (Maternal Dose 250 Mg/day)
  • Nitrazepam (Maternal Dose 5 Mg/day)
  • Tegretol (Maternal Dose 120 Mg/day)
Although Aleviatin demonstrated significant improvements in a number of clinically relevant cases, troublesome symptoms, such as Hypospadias, may still occur.
Aleviatin Side Effect Report#5054665-4
Aspartate Aminotransferase Increased, Blood Albumin Decreased, Blood Lactate Dehydrogenase Increased, C-reactive Protein Increased, Cell Marker Increased, Chest X-ray Abnormal, Fibrin D Dimer Increased, Fibrin Degradation Products Increased, Gamma-glutamyltransferase Increased
This Aspartate Aminotransferase Increased problem was reported by a physician from Japan. A 71-year-old male patient (weight: NA) was diagnosed with the following symptoms/conditions: convulsion,constipation. On
Apr 01, 2006 this consumer started treatment with Aleviatin (dosage: 250 Mg/day). The following drugs were being taken at the same time:
  • Magnesium Oxide (1.5 G/day)
  • Lac B (3 G/day)
  • Tegretol (300 Mg/day)
When using Aleviatin, the patient experienced the following unwanted symptoms/side effects: Aspartate Aminotransferase Increased, Blood Albumin Decreased, Blood Lactate Dehydrogenase Increased, C-reactive Protein Increased, Cell Marker Increased, Chest X-ray Abnormal, Fibrin D Dimer Increased, Fibrin Degradation Products Increased, Gamma-glutamyltransferase IncreasedAlthough 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.
Aleviatin Side Effect Report#4982995-0
C-reactive Protein Increased, Decreased Activity, Hypothermia, Platelet Count Decreased, Urinary Tract Infection, White Blood Cell Count Increased
This C-reactive Protein Increased side effect was reported by a physician from Japan. A 39-year-old male patient (weight:NA) experienced the following symptoms/conditions: epilepsy.The patient was prescribed Aleviatin (drug dosage: NA), which was initiated on
Mar 03, 2006. Concurrently used drugs:
  • Primidone
  • Depakene
  • Lioresal (5 Mg, Qd)
  • Lioresal (5 Mg, Tid)
.After starting to take Aleviatin the consumer reported adverse symptoms, such as: C-reactive Protein Increased, Decreased Activity, Hypothermia, Platelet Count Decreased, Urinary Tract Infection, White Blood Cell Count IncreasedThese side effects may potentially be related to Aleviatin.
Aleviatin Side Effect Report#4964378-2
C-reactive Protein Increased, Decreased Activity, Hypothermia, Platelet Count Decreased, Urinary Tract Infection, White Blood Cell Count Increased
This is a report of a 39-year-old male patient (weight: NA) from Japan, suffering from the following health symptoms/conditions: epilepsy, who was treated with Aleviatin (dosage: NA, start time:
Mar 03, 2006), combined with:
  • Primidone
  • Depakene
  • Lioresal (5 Mg, Qd)
  • Lioresal (5 Mg, Tid)
and developed a serious reaction and side effect(s): C-reactive Protein Increased, Decreased Activity, Hypothermia, Platelet Count Decreased, Urinary Tract Infection, White Blood Cell Count Increased after the beginning of treatment. This case can indicate the possible existence of increased vulnerability to Aleviatin treatment in male patients, resulting in C-reactive Protein Increased side effect.
Aleviatin Side Effect Report#4845039-7
Alanine Aminotransferase Increased, Aspartate Aminotransferase Increased, Blood Pressure Decreased, Candidiasis, Cerebral Infarction, Depressed Level Of Consciousness, Dysphagia, Eating Disorder, Gamma-glutamyltransferase Increased
This report suggests a potential Aleviatin Alanine Aminotransferase Increased side effect(s) that can have serious consequences. A 71-year-old male patient (weight: NA) from Japan was diagnosed with the following symptoms/conditions: convulsion,pneumonia,prophylaxis and used Aleviatin (dosage: NA) starting
Jul 21, 2005. After starting Aleviatin the patient began experiencing various side effects, including: Alanine Aminotransferase Increased, Aspartate Aminotransferase Increased, Blood Pressure Decreased, Candidiasis, Cerebral Infarction, Depressed Level Of Consciousness, Dysphagia, Eating Disorder, Gamma-glutamyltransferase IncreasedAdditional drugs used concurrently:
  • Modacin
  • Omepral
  • Pepcid
  • Targocid
  • Targocid
  • Targocid
  • Targocid
  • Radicut
The patient was hospitalized. Although Aleviatin demonstrated significant improvements in a number of clinically relevant cases, troublesome symptoms, such as Alanine Aminotransferase Increased, may still occur.
Aleviatin Side Effect Report#4673265-9
Epilepsy
This Epilepsy problem was reported by a pharmacist from . A 21-year-old male patient (weight: NA) was diagnosed with the following symptoms/conditions: epilepsy. On
Mar 03, 2005 this consumer started treatment with Aleviatin (dosage: NA). The following drugs were being taken at the same time:
  • Phenobarbital
  • Zaditen (2 Mg/day)
When using Aleviatin, the patient experienced the following unwanted symptoms/side effects: EpilepsyAlthough all drugs are carefully tested before they are licensed for use, they carry side effect risks. Some side effects, such as Epilepsy, may become evident only after a product is in use by the general population.
Aleviatin Side Effect Report#4604911-3
Epilepsy
This Epilepsy side effect was reported by a pharmacist from . A 21-year-old male patient (weight:NA) experienced the following symptoms/conditions: epilepsy.The patient was prescribed Aleviatin (drug dosage: NA), which was initiated on NS. Concurrently used drugs:
  • Phenobarbital
  • Zaditen
.After starting to take Aleviatin the consumer reported adverse symptoms, such as: EpilepsyThese side effects may potentially be related to Aleviatin.



The appearance of Aleviatin 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.

    Aleviatin 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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    More About Aleviatin

    Side Effects reported to FDA: 16

    Aleviatin safety alerts: No

    Reported deaths: 2

    Reported hospitalizations: 6

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