🍽️ cytarabine,(prescription)

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  1. Antineoplastic Activity: Cytarabine belongs to a class of medications known as antimetabolites, which work by interfering with DNA synthesis and inhibiting the growth and replication of cancer cells. Cytarabine is a nucleoside analog that is incorporated into DNA during the S-phase of the cell cycle, leading to DNA strand breaks and inhibition of DNA synthesis. This ultimately results in cell cycle arrest and apoptosis (programmed cell death) of cancer cells.

  2. Treatment of Acute Myeloid Leukemia (AML): Cytarabine is a cornerstone of induction chemotherapy regimens for the treatment of newly diagnosed acute myeloid leukemia (AML), a type of blood cancer characterized by the rapid proliferation of immature myeloid cells in the bone marrow. Cytarabine is often used in combination with other chemotherapy drugs such as anthracyclines (e.g., daunorubicin) or cytarabine plus anthracycline-based regimens (e.g., "7+3" regimen) to induce remission and achieve a complete response in patients with AML.

  3. Treatment of Acute Lymphoblastic Leukemia (ALL): Cytarabine may also be used in the treatment of acute lymphoblastic leukemia (ALL), a type of blood cancer that affects lymphoid cells. It is often used in combination with other chemotherapy agents as part of induction, consolidation, or maintenance therapy regimens for ALL, particularly in pediatric patients. Cytarabine-based chemotherapy regimens help to eradicate leukemic cells from the bone marrow and achieve long-term remission in patients with ALL.

  4. Treatment of Non-Hodgkin's Lymphoma (NHL): Cytarabine may be used in the treatment of certain types of non-Hodgkin's lymphoma (NHL), particularly aggressive subtypes such as diffuse large B-cell lymphoma (DLBCL) or Burkitt lymphoma. It may be used as part of combination chemotherapy regimens to induce remission, reduce tumor burden, and improve survival outcomes in patients with NHL.

  5. Dosage and Administration: Cytarabine is typically administered intravenously (IV) or subcutaneously (SC) by a healthcare professional in a hospital or clinic setting. The dosage and schedule of administration depend on factors such as the type of cancer being treated, the patient's overall health, and their response to treatment. Cytarabine is often given in cycles, with rest periods between doses to allow the body to recover from side effects.

  6. Side Effects: Common side effects of cytarabine may include nausea, vomiting, diarrhea, mucositis (inflammation of the mucous membranes), bone marrow suppression (resulting in low blood cell counts), hair loss, fatigue, and increased risk of infection. Cytarabine can also cause neurotoxicity, particularly at high doses or with prolonged use, leading to neurological symptoms such as headache, confusion, seizures, and cerebellar dysfunction.

  7. Long-term Effects: Cytarabine treatment may be associated with long-term effects such as increased risk of secondary malignancies, particularly therapy-related myeloid neoplasms (t-MN) or myelodysplastic syndromes (MDS), as well as infertility and reproductive toxicities. Patients should be informed about the potential long-term effects of cytarabine therapy and may require long-term monitoring for late-onset complications.

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Impacted of cytarabine,(prescription) On Probiotics

Rank Probiotic Impact
species Akkermansia muciniphila Reduces
species Bifidobacterium adolescentis Reduces
species Bifidobacterium longum Reduces
species Lacticaseibacillus paracasei Reduces
subspecies Bifidobacterium longum subsp. infantis Reduces
subspecies Bifidobacterium longum subsp. longum Reduces

Bacteria Impacted by cytarabine,(prescription)

We extend modifiers to include items that changes the parent and child taxa. I.e. for a species, that would be the genus that is belongs to and the strains in the species.

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Taxonomy Rank Effect Citations Notation
Mediterraneibacter genus Decreases 👪 Source Study
Thomasclavelia genus Decreases 👪 Source Study
Akkermansia genus Decreases 👪 Source Study
Lacrimispora genus Decreases 👪 Source Study
Bifidobacterium genus Decreases 👪 Source Study
Bacteroides genus Decreases 👪 Source Study
Fusobacterium genus Decreases 👪 Source Study Periodontal disease, Lemierre syndrome, skin ulcers
Lacticaseibacillus genus Decreases 👪 Source Study
Blautia genus Decreases 👪 Source Study
Clostridioides genus Decreases 👪 Source Study
unclassified Robinsoniella no rank Decreases ⚗️ Source Study
unclassified Fusobacterium no rank Decreases ⚗️ Source Study
unclassified Negativicoccus no rank Decreases ⚗️ Source Study
Eggerthellales order Decreases ⚗️ Source Study
[Ruminococcus] gnavus species Decreases 📓 Source Study
Thomasclavelia ramosa species Decreases 📓 Source Study
[Ruminococcus] torques species Decreases 📓 Source Study
Akkermansia muciniphila species Decreases 📓 Source Study
Bifidobacterium adolescentis species Decreases 📓 Source Study
Lacrimispora saccharolytica species Decreases 📓 Source Study
Bacteroides fragilis species Decreases 📓 Source Study H02076 Bacteroides infection
Anaerofustis stercorihominis species Decreases ⚗️ Source Study
Asaccharospora irregularis species Decreases ⚗️ Source Study
Negativicoccus sp. S5-A15 species Decreases ⚗️ Source Study
Paraprevotella clara species Decreases ⚗️ Source Study
Slackia sp. NATTS species Decreases ⚗️ Source Study
Bifidobacterium longum species Decreases 📓 Source Study
Pseudoflavonifractor capillosus species Decreases ⚗️ Source Study
[Collinsella] massiliensis species Decreases ⚗️ Source Study
Parvibacter caecicola species Decreases ⚗️ Source Study
Fusobacterium nucleatum species Decreases 📓 Source Study Infectious bacteria
Lacticaseibacillus paracasei species Decreases 📓 Source Study
Blautia obeum species Decreases 📓 Source Study
Clostridioides difficile species Decreases 📓 Source Study Colitis
Coriobacterineae suborder Decreases ⚗️ Source Study
Bifidobacterium longum subsp. infantis subspecies Decreases 👶 Source Study
Bifidobacterium longum subsp. longum subspecies Decreases 👶 Source Study
Bifidobacterium longum subsp. suillum subspecies Decreases 👶 Source Study
Fusobacterium nucleatum subsp. nucleatum subspecies Decreases 👶 Source Study
Lacticaseibacillus paracasei subsp. paracasei subspecies Decreases 👶 Source Study
Chlamydiae/Verrucomicrobia group superphylum Decreases ⚗️ Source Study

Impact of cytarabine,(prescription) on Conditions from US National Library of Medicine

A higher number indicates impact on more bacteria associated with the condition and confidence on the impact.

We have X bacteria high and Y low reported. We find that the modifier reduces some and increases other of these two groups. We just tally: X|reduces + Y|Increase = Positive   X|increases + Y|decrease = Negative.

Benefit Ratio:
Numbers above 0 have increasing positive effect.
Numbers below 0 have increasing negative effect.

Condition Positive Impact Negative Impact Benefit Ratio Impact
Acne 0.2 -0.2
ADHD 0.9 0.9
Allergic Rhinitis (Hay Fever) 0.9 0.8 0.13
Allergies 0.5 1.1 -1.2
Allergy to milk products 0.1 0.2 -1
Alopecia (Hair Loss) 0 0
Alzheimer's disease 1 1.2 -0.2
Amyotrophic lateral sclerosis (ALS) Motor Neuron 1.3 0.6 1.17
Ankylosing spondylitis 0.2 1 -4
Anorexia Nervosa 0.2 -0.2
Asthma 0.2 1 -4
Atherosclerosis 0.2 0.3 -0.5
Atrial fibrillation 0.3 0.3 0
Autism 2.7 2.1 0.29
Barrett esophagus cancer 0.1 0.1
Bipolar Disorder 0.1 0.1
Brain Trauma 0.2 0.1 1
Carcinoma 0.3 0.3 0
Celiac Disease 0.1 0.8 -7
Cerebral Palsy 0.5 0.2 1.5
Chronic Fatigue Syndrome 1.3 0.4 2.25
Chronic Kidney Disease 1.5 1.5
Chronic Lyme 0.1 -0.1
Chronic Obstructive Pulmonary Disease (COPD) 0.1 0.1
Chronic Urticaria (Hives) 0.8 -0.8
Coagulation / Micro clot triggering bacteria 0 0
Colorectal Cancer 0.7 0.2 2.5
Constipation 0.1 0 0
Coronary artery disease 0.8 0 0
COVID-19 2.3 2.4 -0.04
Crohn's Disease 1.8 0.9 1
cystic fibrosis 0.3 -0.3
Depression 2.1 1.4 0.5
Dermatomyositis 0.2 -0.2
Eczema 0.8 0.4 1
Endometriosis 0.3 0.3
Eosinophilic Esophagitis 0.1 0.1
Epilepsy 0.9 1.2 -0.33
Fibromyalgia 0.7 0.3 1.33
Functional constipation / chronic idiopathic constipation 0.7 1.1 -0.57
gallstone disease (gsd) 0 0.2 0
Gastroesophageal reflux disease (Gerd) including Barrett's esophagus 0.3 0.1 2
Generalized anxiety disorder 0.9 0.4 1.25
Graves' disease 0.3 0 0
Halitosis 0.2 0.2
Hashimoto's thyroiditis 1.2 0.3 3
Hidradenitis Suppurativa 0.1 0.1
Histamine Issues,Mast Cell Issue, DAO Insufficiency 0.8 0.4 1
hypercholesterolemia (High Cholesterol) 0.6 -0.6
hyperglycemia 1.2 -1.2
Hyperlipidemia (High Blood Fats) 0.5 0.5
hypersomnia 0 0
hypertension (High Blood Pressure 0.6 1.4 -1.33
Hypothyroidism 0.2 -0.2
Hypoxia 0.4 0.4
IgA nephropathy (IgAN) 1 -1
Inflammatory Bowel Disease 2 1.6 0.25
Insomnia 0.2 0.1 1
Intracranial aneurysms 0.2 0.2
Irritable Bowel Syndrome 0.9 0.9 0
Liver Cirrhosis 0.7 0.6 0.17
Long COVID 2.1 1.1 0.91
Lung Cancer 0.6 -0.6
ME/CFS with IBS 0.4 -0.4
ME/CFS without IBS 0.9 0.3 2
Menopause 0.7 0.7
Metabolic Syndrome 1.7 2.2 -0.29
Mood Disorders 2.6 1.4 0.86
multiple chemical sensitivity [MCS] 0.3 0 0
Multiple Sclerosis 1.3 0.4 2.25
Multiple system atrophy (MSA) 0.9 0.2 3.5
Neuropathy (all types) 0.3 0.3
Nonalcoholic Fatty Liver Disease (nafld) Nonalcoholic 0 1.7 0
NonCeliac Gluten Sensitivity 0.2 -0.2
Obesity 2 1.4 0.43
obsessive-compulsive disorder 0.5 2.3 -3.6
Osteoarthritis 1.5 1.5
Osteoporosis 0.1 0.7 -6
Parkinson's Disease 1 0.3 2.33
Polycystic ovary syndrome 0.2 0.5 -1.5
Postural orthostatic tachycardia syndrome 0.2 -0.2
Premenstrual dysphoric disorder 0.2 0.2
Psoriasis 0.7 0.7 0
rheumatoid arthritis (RA),Spondyloarthritis (SpA) 1.5 0.6 1.5
Rosacea 0.8 0.8
Schizophrenia 1.6 0.2 7
Sjögren syndrome 0 0.9 0
Sleep Apnea 0.3 0.2 0.5
Small Intestinal Bacterial Overgrowth (SIBO) 0.1 0.1 0
Stress / posttraumatic stress disorder 0.6 0.9 -0.5
Systemic Lupus Erythematosus 1.3 0.2 5.5
Tic Disorder 0.2 -0.2
Tourette syndrome 0.3 0.1 2
Type 1 Diabetes 0.4 0.5 -0.25
Type 2 Diabetes 1.7 1.6 0.06
Ulcerative colitis 0.4 1.2 -2
Unhealthy Ageing 2 0.5 3

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