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BURNING SENSATION and Lyrica

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BURNING SENSATION Symptoms and Causes

What is chlamydia?

Chlamydia is a common sexually transmitted disease. It is caused by bacteria called Chlamydia trachomatis. It can infect both men and women. Women can get chlamydia in the cervix, rectum, or throat. Men can get chlamydia in the urethra (inside the penis), rectum, or throat.

How do you get chlamydia?

You can get chlamydia during oral, vaginal, or anal sex with someone who has the infection. A woman can also pass chlamydia to her baby during childbirth.

If you've had chlamydia and were treated in the past, you can get re-infected if you have unprotected sex with someone who has it.

Who is at risk of getting chlamydia?

Chlamydia is more common in young people, especially young women. You are more likely to get it if you don't consistently use a condom, or if you have multiple partners.

What are the symptoms of chlamydia?

Chlamydia doesn't usually cause any symptoms. So you may not realize that you have it. People with chlamydia who have no symptoms can still pass the disease to others. If you do have symptoms, they may not appear until several weeks after you have sex with an infected partner.

Symptoms in women include

  • Abnormal vaginal discharge, which may have a strong smell
  • A burning sensation when urinating
  • Pain during intercourse

If the infection spreads, you might get lower abdominal pain, pain during sex, nausea, or fever.

Symptoms in men include

  • Discharge from your penis
  • A burning sensation when urinating
  • Burning or itching around the opening of your penis
  • Pain and swelling in one or both testicles (although this is less common)

If the chlamydia infects the rectum (in men or women), it can cause rectal pain, discharge, and/or bleeding.

How do I know if I have chlamydia?

There are lab tests to diagnose chlamydia. Your health care provider may ask you to provide a urine sample. For women, providers sometimes use (or ask you to use) a cotton swab to get a sample from your vagina to test for chlamydia.

Who should be tested for chlamydia?

You should go to your health provider for a test if you have symptoms of chlamydia, or if you have a partner who has a sexually transmitted disease. Pregnant women should get a test when they go to their first prenatal visit.

People at higher risk should get checked for chlamydia every year:

  • Sexually active women 25 and younger
  • Older women who have new or multiple sex partners, or a sex partner who has a sexually transmitted disease
  • Men who have sex with men (MSM)
What are the complications of chlamydia?

In women, an untreated infection can spread to your uterus and fallopian tubes, causing pelvic inflammatory disease (PID). PID can cause permanent damage to your reproductive system. This can lead to long-term pelvic pain, infertility, and ectopic pregnancy. Women who have had chlamydia infections more than once are at higher risk of serious reproductive health complications.

Men often don't have health problems from chlamydia. Sometimes it can infect the epididymis (the tube that carries sperm). This can cause pain, fever, and, rarely, infertility.

Both men and women can develop reactive arthritis because of a chlamydia infection. Reactive arthritis is a type of arthritis that happens as a "reaction" to an infection in the body.

Babies born to infected mothers can get eye infections and pneumonia from chlamydia. It may also make it more likely for your baby to be born too early.

Untreated chlamydia may also increase your chances of getting or giving HIV/AIDS.

What are the treatments for chlamydia?

Antibiotics will cure the infection. You may get a one-time dose of the antibiotics, or you may need to take medicine every day for 7 days. Antibiotics cannot repair any permanent damage that the disease has caused.

To prevent spreading the disease to your partner, you should not have sex until the infection has cleared up. If you got a one-time dose of antibiotics, you should wait 7 days after taking the medicine to have sex again. If you have to take medicine every day for 7 days, you should not have sex again until you have finished taking all of the doses of your medicine.

It is common to get a repeat infection, so you should get tested again about three months after treatment.

Can I prevent chlamydia?

The only sure way to prevent chlamydia is to not have vaginal, anal, or oral sex.

Correct usage of latex condoms greatly reduces, but does not eliminate, the risk of catching or spreading chlamydia.

Centers for Disease Control and Prevention

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Lyrica Side Effects

Dizziness (2971)
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Weight Increased (2413)
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Feeling Abnormal (1476)
Fall (1266)
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Burning Sensation (392)
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Recent Reviews

<span style='font-family: Arial;'>I was subscribed Lyrica for my fibromyalgia and took it for about 3 weeks and as a result I ended up jumping through a window (resulting in permanent injuries) and wound up in a mental inst

Extreme fatigue, sleeplessness, short term memory and speech difficulties, Edema, weight gain, stumbling, shortness of breath, numbness in both legs, and completely kills ability to achieve orgasm.

After a little over 2 weeks on Lyrica I awoke one morning with blurred vision. It has been almost 2 weeks and even after stopping the Lyrica I still can not focus my eyes. I am told that my eyes are focusing in and out and if I try hard enough I get

After one dose of 50mg felteuphoric, dizzy,out of touch with reality and extremely depressed; unable to functionas normal.great for pain but don't think I can continue withthis.

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BURNING SENSATION 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 A Placebo-Controlled Trial of Pregabalin (Lyrica) for Irritable Bowel Syndrome
Condition: Irritable Bowel Syndrome
Interventions: Drug: Pregabalin (Lyrica);   Drug: Placebo
Outcome Measures: Primary aim: Collect preliminary data comparing effects of Pregabalin and placebo on abdominal pain/discomfort on bowel symptom score (BSS), overall BSS score, and adequate relief of irritable bowel syndrome (IBS) symptoms in patients with IBS;   To compare the effect of Pregabalin and placebo on self-reported overall and individual BSS scores;   compare effect of Pregabalin and placebo on adequate relief of IBS pain or discomfort at least 50% of the time;   To compare effect of Pregabalin and placebo on overall and individual BSS scores;   To compare the effect of Pregabalin and placebo on the proportion of patients with at least 3 point changes in 11 point pain and IBS scores
2 Recruiting A Study of Pregabalin (Lyrica) Augmentation in Serotonin Reuptake Inhibitor-Refractory Obsessive Compulsive Disorder
Condition: Obsessive-Compulsive Disorder
Interventions: Drug: pregabalin;   Drug: Placebo
Outcome Measures: Yale-Brown-Obsessive-Compulsive-Scale;   Clinical Global Impression - Improvement;   Montgomery Asberg Depression Rating Scale;   Sheehan Disability Scale;   Beck Depression Inventory;   Clinical Global Impression - Severity;   Saving Inventory - Revised;   Dimensional Yale-Brown-Obsessive Compulsive Scale (D-Y-BOCS);   Padua Inventory
3 Not yet recruiting Efficacy and Safety of KW21052 Compared to Lyrica in the Diabetic Patients With Neuropathic Pain
Condition: Diabetic Neuropathy
Interventions: Drug: KW21052;   Drug: Lyrica;   Drug: Lyrica (low dose);   Drug: Placebo of KW21052;   Drug: Placebo of Lyrica
Outcome Measures: Numerical pain rating scale (NRS);   Change on on the numerical pain rating scale (NRS);   Response rate;   Clinical Global Impression of Change (CGIC);   Improved quality of life (QoL);   Drug compliance;   Adverse events
4 Recruiting The Effects of Pregabalin on Postoperative Pain After Cardiac Surgery
Condition: Postoperative Pain
Interventions: Drug: Pregabalin 75mg;   Drug: pregabalin 150 mg;   Drug: Placebo
Outcome Measures: opioid consumption and other analgesics after surgery;   Remaining surgery related pain and analgesics consumption
5 Unknown  Imipramine and Pregabalin Combination in Painful Polyneuropathy
Condition: Polyneuropathy
Interventions: Drug: Imipramine;   Drug: Pregabalin;   Drug: Imipramine, pregabalin;   Drug: Placebo
Outcome Measures: Total pain intensity as measured by numeric rating scale 0-10 points.;   Verbal pain relief scale with 6 classes;   Specific pain symptom rated by numeric rating scales 0-10 points;   Rating of evoked pains symptoms (pressure, brush, repetitive pin-prick, cold) as measured by numeric rating scales 0-10 points;   Sleep disturbance as measured by numeric rating scale 0-10 points;   Consumption of escape medication (number of tablets of paracetamol);   Health related quality of life (SF-36);   Major Depression Inventory (MDI)
6 Recruiting A Study Evaluating the Efficacy and Safety of Pregabalin Against Frequent Muscle Cramp in Patients With Liver Cirrhosis
Conditions: Muscle Cramp;   Liver Cirrhosis
Interventions: Drug: Pregabalin;   Drug: Placebo
Outcome Measures: mean reduction rates of the frequency of muscle cramps between pregabalin and placebo groups;   Response rates , Mean change in the average cramp pain intensity , peripheral nerve excitability , the quality of life, quality of sleep , safety
7 Recruiting A Safety, Efficacy and Tolerability Trial of Pregabalin as Add-On Treatment in Pediatric and Adult Subjects With Primary Generalized Tonic-Clonic (i.e., Grand Mal) Seizures.
Condition: Generalized Tonic Clonic Seizures
Interventions: Drug: Pregabalin Dose Level 1;   Drug: Pregabalin Dose Level 2;   Drug: Placebo
Outcome Measures: Percent reduction of 28 day seizure rate for all PGTC seizures relative to placebo during the double blind assessment phase.;   Responder rate, defined as the proportion of subjects who had at least a 50% reduction in 28 day PGTC seizure.
8 Unknown  Efficacy of Pregabalin in the Management of Chronic Uremic Pruritus
Condition: Uremic Pruritus
Interventions: Drug: Pregabalin;   Drug: Placebo
Outcome Measures: Reduction of UP by more than 50% after Pregabalin administration;   Reduction of chronic pain of various origin and improvement in insomnia after Pregabalin administration
9 Recruiting Study To Evaluate Efficacy, Safety And Tolerability Of Lyrica In Patients With Painful Diabetic Peripheral Neuropathy
Condition: Diabetic Neuropathy, Painful
Interventions: Drug: Pregabalin;   Drug: Placebo matched with pregabalin
Outcome Measures: Endpoint mean pain score based on the pain scores from the subject's daily pain rating scale;   Weekly mean pain scores from the subject's daily pain rating scale;   Weekly mean sleep interference scores from the subject's daily sleep interference scale;   Responder rates with at least a 30% reduction from baseline in weekly mean pain score;   Change from baseline in Short-Form McGill Pain Questionnaire at week 9;   Change from baseline in Pain Visual Analogue Scale at week 9;   Change from baseline in Medical Outcomes Study -Sleep Scale at week 9;   The Subject Global Impression of Change at week 9;   The Clinical Global Impression of Change at week 9;   Change from baseline in Hospital Anxiety and Depression Scale at week 9
10 Recruiting Effects of Pregabalin on Post-cesarean Pain
Condition: Uncomplicated Singleton Pregnancies
Interventions: Drug: Placebo;   Drug: Pregabalin 300 mg group;   Drug: Pregabalin 150 mg group
Outcome Measures: cumulative patient controlled morphine consumptions;   postoperative pain scores;   neonatal Apgar scores;   Neurologic and adaptive capacity scores;   Maternal sedation;   Maternal nausea and vomiting
11 Recruiting Safety, Tolerability and Preliminary Efficacy of AZD5213 in Combination With Pregabalin in Subjects With PDN and Good Pain Reporting Ability
Condition: Diabetic Neuropathy, Painful; Diabetic Neuropathies
Interventions: Drug: AZD5213 + pregabalin;   Drug: Placebo;   Drug: pregabalin capsules
Outcome Measures: Change in Item 5 of Brief Pain Inventory Diabetic Peripheral Neuropathy version (BPI-DPN);   Incidence and severity of Treatment Emergent Adverse Events;   Vital signs ( blood pressure, heart rate, weight and temperature);   Clinical Laboratory Evaluations;   Medical Outcomes Study (Revised) Sleep Scale (MOS-R);   Columbia Suicide Severity Rating Scale (CSSR-S);   Neuropathic Pain Symptom Inventory (NPSI);   Sleep Interference Scale (SIS)
12 Unknown  Perioperative Administration of Pregabalin for Pain After Septoplasty
Condition: Deviated Nasal Septum
Interventions: Drug: Pregabalin (Lyrica);   Drug: Vitamin complex (placebo)
Outcome Measures: Pain score (Verbal numerical rating scale, VNRS and Visual Analogue Scale, VAS);   The number of patients with side effects including Nausea and vomiting, sedation, headache, dizziness;   The number of patients who required additional analgesics during admission
13 Not yet recruiting Pregabalin for the Treatment and Prevention of Spinal Cord Injury Neuropathic Pain
Conditions: Neuropathic Pain;   Spinal Cord Injuries
Interventions: Drug: Pregabalin;   Drug: Placebo
Outcome Measures: Daily at-level non-evoked pain intensity measured with the numerical rating scale (0-10) expressed as the mean 7-day pain intensity;   Weekly below-level non-evoked pain intensity measured with the numerical rating scale (0-10);   Weekly evaluation of at-level neuropathic pain symptoms using the "Neuropathic Pain Symptoms Inventory" (NPSI);   Weekly evaluation of at-level neuropathic pain intensity and interference using the "Brief Pain Inventory" (BPI);   Weekly evaluation of the change in at-level non-evoked neuropathic pain using the "Patient Global Impression Change" (PGIC);   Weekly evaluation of anxiety and depression using the Hospital Anxiety and Depression Scale (HADS);   Weekly evaluation of spasm frequency below the spinal cord injury using the Penn questionnaire;   Measurement of the amplitude of cold and heat sensory evoked potentials (Cz-Fz) studied above (C4) and at-level of the SCI;   Serum TNF-R1 level;   Weekly at-level non-evoked pain intensity measured with the numerical rating scale (0-10) 28 days after the termination of the clinical trial;   Number of Paracetamol tablets used as rescue medication during the week;   Prevalence and type of adverse events in patients treated with pregabalin;   Unblinding testing: patient and investigator will be asked for the treatment they think to have received. Reasons for their judgement (efficacy and safety) will also be asked.
14 Recruiting Adolescent Fibromyalgia Study
Condition: Fibromyalgia
Interventions: Drug: placebo;   Drug: pregabalin (Lyrica)
Outcome Measures: Endpoint mean pain score from daily pain diary;   Endpoint mean sleep quality score from the daily sleep diary;   Pain Numeric Rating Scale (Pain-NRS) at Termination Visit;   Patient Global Impression of Change at Termination;   Parent Global Impression of Change at Termination Visit;   Fibromyalgia Impact Questionnaire for Children at Termination Visit;   Frequency and severity of adverse events at every visit.;   Physical and neurological exams.;   Vital signs.;   Suicidality Tracking Scale (STS).;   12-Lead Electrocardiogram (ECG).;   Laboratory tests: hematology, chemistry, serum pregnancy, urinalysis.;   Reproductive hormone monitoring (females only);   Tanner staging-assessment of pubertal status (females only);   Pharmacokinetic endpoint: A population pharmacokinetic analysis will be performed using the sparse PK samples obtained at V6.
15 Recruiting Effect of Pregabalin in Patients With Radiation-Induced Peripheral Neuropathic Pain
Condition: Neuropathic Pain
Interventions: Drug: Pregabalin;   Drug: Placebo
Outcome Measures: Daily Pain Rating Scale (DPRS) at week 12;   The modified Brief Pain Inventory-short form (mBPI);   Daily Sleep Interference Scale(DSIS)
16 Unknown  Efficacy of Pre-operative Oral Pregabalin in Ambulatory Inguinal Hernia Repair for Post Operative Pain
Conditions: Inguinal Hernia;   Postoperative Pain
Intervention: Drug: Pregabalin
Outcome Measures: Study is constructed to determine whether the use of oral pregabalin premedication to assess the analgesic efficacy for post operative pain at Alert, 15, 30, 45, 60 and 120 min, Day 1, Day 2 and Day 3.;   Opiod Sparing;   Side effect of medication
17 Not yet recruiting Exploratory Study on the Use of Pregabalin for the Treatment of Taxol Related Arthralgia-Myalgia
Conditions: Taxane;   Drug-related Side Effects and Adverse Reactions;   Pain;   Breast Cancer
Interventions: Drug: Pregabalin;   Drug: Placebo
Outcome Measures: Integrated Numeric Pain Scores and Rescue Analgesic Medication Requirement as calculated by the method proposed by Silverman et al (Silverman, O'Connor et al. 1993).;   Numeric Pain Score (NPS);   The additional number of hours spent in horizontal position (∆HHP**);   FACT-taxane score
18 Recruiting Evaluation of Preoperative Use of Pregabalin on Postoperative Analgesia After Laparoscopic Colorectal Surgery
Condition: Postoperative Pain
Interventions: Drug: Pregabalin;   Drug: Placebo;   Drug: Morphine
Outcome Measures: Postoperative opioid consumption;   Postoperative pain;   Side- effects;   Chronic Pain;   Hospital stay
19 Unknown  Randomized Study of Pregabalin for Pain Reduction in Patients With Rest Pain and Lower Limb Ischemia
Conditions: Critical Limb Ischemia;   Arterial Occlusive Disease;   Pain;   Ischemia
Interventions: Drug: pregabalin;   Drug: placebo
Outcome Measures: Reduction in Rating Scale (RS) pain compared to baseline. RS Pain will be assessed at 7, 14 days for all participants and after 28 and 56 days for patients continuing the extended phase of study.;   Improvement in the Short Form 36 (SF-36) parameter "bodily pain".;   The amount, dose and duration of concomitant pain medication use during study compared to use before study.;   Safety outcomes and adverse events will be examined and recorded throughout the study. Patient reported dizziness will be recorded separately in the CRF, as well as blood pressure at visits.
20 Unknown  Pain Relief Following Arthroscopic Rotator Cuff Repair: Perioperative Pregabalin Administration Versus Interscalene Brachial Plexus Block
Condition: Pain
Interventions: Drug: Pregabalin;   Procedure: ISBPB - interscalene brachial plexus block
Outcome Measure: To compare postoperative pain relief by pregabalin versus ISBPB following arthroscopic rotator cuff repair