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HEART RATE INCREASED and Methotrexate

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HEART RATE INCREASED Symptoms and Causes

An arrhythmia is a problem with the rate or rhythm of your heartbeat. It means that your heart beats too quickly, too slowly, or with an irregular pattern. When the heart beats faster than normal, it is called tachycardia. When the heart beats too slowly, it is called bradycardia. The most common type of arrhythmia is atrial fibrillation, which causes an irregular and fast heart beat.

Many factors can affect your heart's rhythm, such as having had a heart attack, smoking, congenital heart defects, and stress. Some substances or medicines may also cause arrhythmias.

Symptoms of arrhythmias include

  • Fast or slow heart beat
  • Skipping beats
  • Lightheadedness or dizziness
  • Chest pain
  • Shortness of breath
  • Sweating

Your doctor can run tests to find out if you have an arrhythmia. Treatment to restore a normal heart rhythm may include medicines, an implantable cardioverter-defibrillator (ICD) or pacemaker, or sometimes surgery.

NIH: National Heart, Lung, and Blood Institute

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HEART RATE INCREASED treatment research studies

Methotrexate clinical trials, surveys and public health registries


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Methotrexate Side Effects

Pyrexia (411)
Pancytopenia (356)
Nausea (321)
Pneumonia (304)
Arthralgia (271)
Headache (269)
Injection Site Pain (265)
Rheumatoid Arthritis (260)
Dyspnoea (248)
Mucosal Inflammation (241)
Diarrhoea (238)
Vomiting (231)
Fatigue (223)
Asthenia (198)
Cough (196)
Sepsis (195)
Anaemia (195)
Pain (188)
Renal Failure Acute (177)
Malaise (156)
Febrile Neutropenia (152)
Abdominal Pain (152)
Injection Site Erythema (145)
Pain In Extremity (141)
Convulsion (139)
Rash (139)
Neurotoxicity (138)
Dizziness (131)
Neutropenia (129)
Condition Aggravated (129)
Thrombocytopenia (127)
Toxicity To Various Agents (125)
Oedema Peripheral (121)
Alanine Aminotransferase Increased (121)
Renal Failure (118)
Hypertension (115)
Weight Decreased (114)
Erythema (113)
Interstitial Lung Disease (113)
Stomatitis (108)
Respiratory Failure (108)
Bone Marrow Failure (108)
Leukopenia (104)
Fall (103)
Infection (103)
Aspartate Aminotransferase Increased (99)
Hypotension (95)
Nasopharyngitis (93)
Paraesthesia (93)
Septic Shock (91)

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Recent Reviews

Hi I haven't had any side effects for the past six years of Methotrexate. but recently I am having some stomach discomfort like as soon as i eat something i have the slight discomfort on my abdoman. I take a glass of green leaf juice and i am fine ag

I am 60 Years of age. 8 years ago i was falsely diagnosed with Rheumatoid Arthritis, i was started on Methoblastin 5Mg a week, Was not given Folic Acid and Ranitidine within the 5 months of taking the tablets i developed exposed blood vessels and spo

I have been on methotrexate for almost months and last two weeks have had severe pains at times lower back , It feel like the kidneys because one side hurts at times and in the mornings it is worse. I am 3 days shy of talking another blood test. Is

I just started Methotrexate, I started itching in the same areas where I had experienced itching with the chicken pox 2 years ago. I am a 51 year old female who contracted chicken pox at 49 years old. This frightens me as I know this can cause diss

I only took it for 21 days but in that time, it put me into a full panic attack that lasted almost 8 days after I went off the medication. I had mental confusion, could not speak properly (I knew what I wanted to say but the words would not come out

I was diagnosed with Rheumatoid Arthritis about 4 years ago when I was 13 or 14, they looked at me and said I had it, they didn't do any blood tests and when they did, nothing showed. But they started me on about 5 mg of Methotrexate, Prednisone, and

Im a 44yrs old female who took methotrexate for 2yrs with excellent results and no side effects but had to stop taking it when it started lowering my white cells.

My 27 years of MTX therapy have prevented physical deformity but caused me to have damage to my lungs. I am short of breath on any activity. MTX helped the pain somewhat but at the cost of my lungs? I was never told about this possibility nor told it

Painful cough after 2 days of 1st dose lasting-- to date-- 6 days

What did you have?

Yesterday, after taking Sam-e with Glucosamine. I got a pain between my shoulder blade, jaw pain, dizziness, sweating. felt like a heart attack. I did not go to the hospital because of the money needed. No ins

I took chapmix over 2 years ago and have been smoke free ever since, which I am very pleased about. However, I have had some issues with my heart, starting about a year ago with irregular, very rapid heartbeats. Finally I went through a whole

After using Clobetasol for a two week cycle, my doctor suggested I use it one day during the week, applying it twice that day. Since that time, I have experinced severe chest pain. I recently saw my doctor for heart attack symptoms before I reali

i had heart failure last august 2010, among other tablets i have been taking emconcor. i wonder whether these tablets are responsible for making my limbs feel weak, and lightheaded.

I HAD 1 SHOT OF THIS AND WITHIN 12 HOURS I WENT FROM A VERY NORMAL BLOOD PRESSURE TO WAKING AT 5 A.M. NEXT DAY WITH 198/110 AND 104 PULSE RATE. IT HAS CONTINUED ALL WEEK AFTER AND I'M NOW ON A BLOOD PRESSURE DRUG TO TRY AND CONTROL IT. EVEN WITH DR

I have been put on Molipaxin 3 weeks ago, I have dry mouth, hair loss and my panic attacks were showing no signs of improvement. Dr increased it to 100mg and put me onto Lamictin. I am not bi polar nor epileptic. My disorder ist algora phoebia. I a

Side effects I have from Nadolol are confusion, dizziness, lightheaded, increased depression and anxiety, and mild nausea.

I am real tired I've been on coreg about two weeks, I don't know if Ican keep taking it. I am so sleepy all the time don't want to do anything my chest hurts. Don't know what to do, if Idon't take it my heart want work right. JUST STUCK

Have taken hydrea for a year because my spleen had increased in size. I have noticed increased loss of memory and some confusion for the past couple of months. I take 500 mg every other day and 1000 mg every other day.

fell dizziness and was admitted. Doc execute with dianostic including blood teat and heart check all. good. Doc make a decision by saying i'm getting Vertigo and treat with BETASERC. Below is the effect after 2 days take this medicine:- I was

HEART RATE INCREASED Clinical Trials and Studies

Treatments might be new drugs or new combinations of drugs, new surgical procedures or devices, or new ways to use existing treatments. The goal of clinical trials is to determine if a new test or treatment works and is safe. Clinical trials can also look at other aspects of care, such as improving the quality of life for people with chronic illnesses. People participate in clinical trials for a variety of reasons. Healthy volunteers say they participate to help others and to contribute to moving science forward. Participants with an illness or disease also participate to help others, but also to possibly receive the newest treatment and to have the additional care and attention from the clinical trial staff.
Rank Status Study
1 Recruiting Individualized High Dose Methotrexate to Treat Cancer in Children Who Have a Significant Risk for Side Effects to Methotrexate
Condition: Cancer
Intervention: Drug: Methotrexate
Outcome Measures: Incidence of success (achieving an end infusion peripheral blood Methotrexate concentration between 50-80 μM);   Incidence of nephrotoxicity;   Incidence of neurotoxicity;   Incidence of mucositis;   Incidence of hepatoxicity;   Incidence of myelosuppression
2 Unknown  Methotrexate and Temozolomide Versus Methotrexate, Procarbazine, Vincristine and Cytarabine
Condition: Lymphoma
Interventions: Drug: Methotrexate and temozolomide;   Drug: Methotrexate , procarbazine ,vincristine ,cytarabine
Outcome Measures: Progression-free survival;   Overall survival:median and overall survival;   Response rates;   Toxicity;   Late toxicity
3 Not yet recruiting The Efficiency Of The Methotrexate At Patients Affected By Grave Pelade
Condition: ALOPECIA AREATA
Intervention: Drug: Methotrexate
Outcome Measures: OUTCOME MESURE;   SECONDARY OUTCOME MEASURE
4 Recruiting A Phase 2b/3 Study to Evaluate Efficacy and Safety of Masitinib in Comparison to Methotrexate in Patients With Active Rheumatoid Arthritis With Inadequate Response to Methotrexate or to Any Disease-Modifying Antirheumatic Drug
Condition: Rheumatoid Arthritis (RA)
Interventions: Drug: masitinib;   Drug: Methotrexate
Outcome Measures: ACR50;   ACR
5 Not yet recruiting The Effects of Methotrexate Therapy on ST Segment Elevation MYocardial InfarctionS (TETHYS Trial)
Condition: Myocardial Infarction
Interventions: Drug: Methotrexate;   Drug: Riboflavin
Outcome Measures: Area under the curve of creatine kinase;   Area under the curve for creatine kinase MB fraction and troponin I high sensitive;   Compare the peaks of CK, CK-MB and troponin I ultra-sensitive;   Compare the levels of high-sensitivity C-reactive protein at admission, after 72 hours and after 3 months;   Compare the levels of erythrocyte sedimentation rate on admission and after 72 hours;   Compare B-type natriuretic peptide (BNP) levels on admission, after 72 hours and after 3 months;   Compare the "TIMI frame count" of the culprit artery;   Compare the Killip score on admission and after 72 hours;   Assess ventricular ejection fraction with transthoracic echocardiography during the first 72 hours after 3 months;   Assess mortality at 3 months;   Evaluate reinfarction in 3 months;   Rate side effects
6 Not yet recruiting VACcination In Methotrexate Treated Rheumatoid Arthritis Patients
Condition: Rheumatoid Arthritis
Interventions: Biological: Prevenar 13;   Biological: Pneumo23;   Drug: Methotrexate
Outcome Measures: rate of immunological positive answer 1 month after antipneumococcal vaccination by the conjugated vaccine Prevenar13 ® in patients suffering from rheumatoid polyarthritis.;   Number of patients in each group who will know fully immunological answer to 5 interest serotypes after the first antipneumococcal vaccination (Prevenar13);   Number of patients in each group who will know an immunological answer to 13 serotypes after the first antipneumococcal vaccination (Prevenar13);   Number of patients who will know a fully immunological answer (13 serotypes of vaccine) after a antipneumococcal revaccination with Pneumo 23.;   Number of patients who will suffer from adverse events in relation with the antipneumococcal vaccination;   Frequency of occurence of disease spurts from the first vaccination until the end of the study;   occurence of the pneumococcal disease from the first vaccination to the end of the study.
7 Recruiting Will the Use of Glucarpidase After Methotrexate Treatment Allow More Patients With Bone Sarcoma to Have Fewer Side Effects and Receive Subsequent Chemotherapy on Time?
Conditions: Osteosarcoma;   Spindle Cell Sarcoma of Bone
Interventions: Drug: Glucarpidase;   Drug: Methotrexate;   Drug: Folinic Acid
Outcome Measures: Estimate of the difference in proportions of patients ready to receive chemotherapy on Day 15 of each chemotherapy cycle comparing standard rescue and glucarpidase+standard rescue;   To investigate whether glucarpidase rescue after high-dose Methotrexate reduces the incidence of Methotrexate associated adverse effects;   Plasma Methotrexate concentration;   Incidence of glucarpidase related adverse effects;   Number of days required in hospital per cycle;   Assessment of quality of life;   Serum anti-glucarpidase IgG levels following glucarpidase administration;   To investigate whether glucarpidase rescue after high-dose Methotrexate reduces the severity of Methotrexate associated adverse effects;   To investigate whether glucarpidase rescue after high-dose Methotrexate reduces the duration of Methotrexate associated adverse effects;   Plasma DAMPA concentration;   Total dose of folinic acid rescue required per cycle
8 Not yet recruiting Methotrexate for Central Serous Chorioretinopathy Treatment Trial
Condition: Central Serous Chorioretinopathy
Interventions: Drug: Methotrexate;   Drug: Delayed treatment
Outcome Measure: Optical Coherence Tomography indicating the level of central serous detachment
9 Recruiting Tac, Mini-MTX, MMF Versus Tac, MTX for GVHD Prevention
Conditions: Chronic Myelogenous Leukemia;   Acute Lymphoblastic Leukemia;   Acute Myeloid Leukemia;   Acute Biphenotypic Leukemia;   Myelodysplastic Syndrome;   Myeloproliferative Neoplasm;   Non-Hodgkin Lymphoma;   Hodgkins Disease;   Chronic Lymphocytic Leukemia;   Multiple Myeloma
Interventions: Drug: tacrolimus;   Drug: Methotrexate;   Drug: Mycophenolate mofetil;   Drug: Methotrexate (low dose)
Outcome Measures: Incidence of severe (grade 3-4) mucositis graded according to the World Health Organization (WHO) grading scale;   Time to neutrophil engraftment;   Time to platelet engraftment;   Incidence of acute GVHD;   Length of hospitalization;   Use of total parenteral nutrition (TPN);   Overall survival defined by Center for International Blood and Marrow Transplant Research (CIBMTR) criteria for individual diseases;   Progression-free survival defined by CIBMTR criteria for individual diseases;   Incidence of chronic GVHD;   Length of time on continuous infusion narcotics;   Incidence of infection;   Incidence of hepatotoxicity;   Incidence of nephrotoxicity;   Incidence of pulmonary toxicity
10 Recruiting Tacrolimus/Methotrexate Versus Cyclosporine/Methotrexate for Prophylaxis of Graft Versus Host Disease
Condition: Graft vs Host Disease
Interventions: Drug: Tacrolimus;   Drug: Cyclosporine;   Drug: Methotrexate
Outcome Measures: incidence of grade II-IV acute graft versus host disease;   incidence of infection;   incidence of adverse drug reactions
11 Recruiting Methotrexate Treatment for Ectopic Pregnancy
Condition: Ectopic Pregnancy
Interventions: Procedure: Single-dose Methotrexate;   Procedure: Two-dose Methotrexate protocol
Outcome Measure: treatment success
12 Recruiting Initial Treatment With Golimumab in Early PsA
Condition: Psoriatic Arthritis
Interventions: Drug: golimumab;   Drug: Methotrexate
Outcome Measures: Percentage of patients achieving DAS remission response criteria;   Number of Participants with Adverse Events;   Number of patients fulfilling Minimal Disease activity criteria and other outcome measurements
13 Recruiting Methotrexate or Dactinomycin in Treating Patients With Low-Risk Gestational Trophoblastic Neoplasia
Conditions: Gestational Trophoblastic Tumor;   Hydatidiform Mole;   Low Risk Metastatic Gestational Trophoblastic Tumor;   Uterine Choriocarcinoma
Interventions: Drug: leucovorin calcium;   Biological: dactinomycin;   Drug: Methotrexate;   Procedure: quality-of-life assessment
Outcome Measures: Complete response vs treatment failure;   Severity of adverse events as assessed by the National Cancer Institute (NCI) Common Terminology Criteria for Adverse Events version 4;   Overall QOL
14 Recruiting A Phase III Study to Evaluate the Efficacy and Safety of ENIA11 in Combination With Methotrexate Versus Methotrexate Alone in Patients With RA
Condition: Rheumatoid Arthritis
Interventions: Drug: Methotrexate;   Drug: ENIA11;   Drug: Placebo
Outcome Measure: ACR20 responder at last treatment visit
15 Recruiting Prospective, Multicentric, Phase II Randomized Controlled Trial on Two Parallel Groups Comparing the Efficacy of Two Immunosuppressive Drugs (Methotrexate, Cyclophosphamide) in Large Granular Lymphocytes Leukemia
Condition: Large Granular Lymphocytes Leukemia
Interventions: Drug: Methotrexate;   Drug: Cyclophosphamide
Outcome Measures: Complete response (CR);   overall response rate (ORR);   Hematological partial response (PR);   Progressive disease;   Time-to-relapse;   Molecular remission;   Adverse events rate;   Compliance;   relationship between the response to treatment and the phenotypic subtype
16 Recruiting Leflunomide Versus Sulfasalazine/Methotrexate in Rheumatoid Arthritis:an Ultrasound/Magnetic Resonance Imaging Study
Condition: Rheumatoid Arthritis
Interventions: Drug: Methotrexate plus sulfasalazine;   Drug: Leflunomide
Outcome Measures: MRI synovitis score;   MRI bone marrow edema score;   MRI erosion score;   US synovitis score;   clinical outcomes
17 Recruiting A Study on the Impact of Methotrexate Discontinuation on the Efficacy of Subcutaneous RoActemra/Actemra (Tocilizumab) With Methotrexate in Patients With Moderate to Severe Active Rheumatoid Arthritis
Condition: Rheumatoid Arthritis
Interventions: Drug: tocilizumab [RoActemra/Actemra];   Drug: Methotrexate;   Drug: placebo
Outcome Measures: Change in disease activity (DAS28) scores;   Change in bone erosion scores for patients in the MRI substudy;   Percentage of patients with a >/= 1.2 worsening in DAS28 between Week 24 and Weeks 40 and 52;   Percentage of patients achieving DAS 28 <2.6 and DAS28 </= 3.2 at Weeks 40 and 52;   Percentage of patients achieving ACR20/50/70 responses at Weeks 40 and 52;   Safety: Incidence of adverse events
18 Recruiting Methotrexate in the Treatment of Chronic Idiopathic Urticaria
Condition: Chronic Urticaria
Interventions: Drug: Methotrexate (Novatrex ®) + anti-H1;   Drug: Placebo + anti-H1
Outcome Measures: Number of patients with complete remission of urticaria at 18 weeks;   Tolerance : clinical and biological safety;   Efficacy of the treatment in improving symptoms : pruritus;   Persistency of the complete remission at 26 weeks;   Efficacy of the treatment in improving symptoms : outbreaks by week;   Efficacy of the treatment in improving symptoms : duration of lesions;   Efficacy of the treatment in improving quality of life;   Efficacy of the treatment in improving quality of sleep;   Efficacy of the treatment in improving facial/cervical urticarial lesions
19 Recruiting High-dose Methotrexate and Liposomal Cytarabine in Treating Patients With CNS Metastases From Breast Cancer
Conditions: Central Nervous System Metastases;   Leptomeningeal Metastases;   Recurrent Breast Cancer;   Stage IV Breast Cancer;   Tumors Metastatic to Brain
Interventions: Drug: Methotrexate;   Drug: liposomal cytarabine;   Other: quality-of-life assessment;   Other: questionnaire administration
Outcome Measures: Progression-free survival (PFS);   Cancer Therapy Evaluation Program (CTEP) Common Toxicity Criteria grade 3+ neurological and systemic toxicity that persists following dose reductions or schedule modifications;   Overall survival;   Duration of response;   Cytologic response as measured by CSF cytology (positive or negative for malignant cells);   FACT-Brain (Br) total score and subscales (physical well-being, social/family well-being, emotional well-being, functional well-being, symptom index) using standard scoring
20 Not yet recruiting Low-dose Methotrexate for Reduction GINA 5 Medications in Chronic Severe Asthma
Condition: Low Dose Methotrexate in Severe Chronic Asthma
Interventions: Drug: Methotrexate;   Drug: Placebo
Outcome Measures: At least 50% reduction in total dosage of GINA step 5 medications;   clinically significant changes in clinimetric scores