Get answers for your health queries from top Doctors for FREE!

100% Privacy Protection

100% Privacy Protection

We maintain your privacy and data confidentiality.

Verified Doctors

Verified Doctors

All Doctors go through a stringent verification process.

Quick Response

Quick Response

All Doctors go through a stringent verification process.

Reduce Clinic Visits

Reduce Clinic Visits

Save your time and money from the hassle of visits.

Ask Free Question

Filters

  • Gender
  • Experience
  • Reviews
  • Questions

Sort

10 Best Anemia Treatment doctors in Pammal

Book appointments with minimal wait times and verified doctor information.

Share

Share this doctor with others via...

Dr. Hariharan V.s Anemia Treatment

Available Today

View
Hariharan's logo

Consult Dr. Hariharan V.s

Questions & Answers on "Anemia Treatment" (101)

I am a 7 month old baby's breastfeeding mother. I had a c section delivery but even after 7 months my body weakness is not getting better. Sometime this weakness is fine and sometimes I feel very weak. Now since last 2 3 days I am feeling dizzy, having constipation, acidity and shortness of breath and my wrist and feet are also trembling sometimes. I thought this is anemic symptoms.

Female | 25

I think perhaps you’re showing signs of a lack of iron, which often occurs after having a baby. You might feel weak, lightheaded, out of breath or have trembling hands and feet. You could also get constipated, have heartburn or feel low. Eating red meat, spinach and lentils can help because they are high in this mineral. You might also need to take an iron supplement. But talk to your doctor to make sure that’s what it is and work out a plan for getting better.

Answered on 4th June '24

Read answer

I went to general check and blood test. I got CEA test level 8.16 I don't smoke or drink. Reason for it. Is it normal

Male | 55

CEA stands for Carcinoembryonic Antigen, a protein produced in the body, and the levels of it in the body may be high because of different causes such as inflammation or infection. Usual symptoms are unusual with a slight increase in CEA levels, but further tests and monitoring are also often necessary. It’s important to visit your healthcare provider to find out the exact reasons for your condition and the best ways to fight it.

Answered on 19th June '24

Read answer

I have test creatine Its having less than 0.4 please suggest me anything required

Female | Srilekha

It's good that creatinine levels are below 0.4. Creatinine is a waste product that your kidneys filter out of your blood. If it's too high, it can mean your kidneys aren't working well. Low creatinine levels can happen if someone has less muscle mass or is malnourished. Make sure you have a balanced diet and avoid a diet high in protein, also, be careful so as not to get dehydrated.

Answered on 9th July '24

Read answer

Hello doctor j have been on medication of malaria but no change J have headec and fever all the body and macle pain j do what now

Male | 24

If you still have a headache, fever, and muscle aches after taking medicine, you might have malaria. The malaria parasite can sometimes resist certain drugs. You should see a doctor immediately so that they can change your treatment and make you feel better. Don't delay—get checked out as soon as possible. 

Answered on 7th June '24

Read answer

Dear Doctor, Due to my father's high blood viscosity, suspicion of polycythemia arises, necessitating blood draws every 3 weeks to maintain appropriate levels. At 69 years old, he experiences symptoms such as skin itching, swelling, head numbness, and fatigue. Currently, his JAK2 V617F mutation showed 0.8 then 1.2%, with JAK2 exon 12 negative and EPO at 13.4. Abdominal CT and chest X-ray are normal. After a few months of phlebotomy, his levels normalized. Now, we await the bone marrow biopsy results, which do not confirm Polycythemia Vera: "Microscopic description: The bone marrow biopsy sample shows somewhat hypocellular hematopoietic parenchyma relative to age, which is terminally mature. Myeloid ratio is 2:1 with dominance of late precursors; no blast cells are noted. The number of megakaryocytes is normal with no clustering. There is no interstitial fibrosis or lymphoid infiltrate. Diagnosis: Mature, hypocellular hematopoietic parenchyma without myeloproliferative features. Cytogenetic analysis confirmed male karyotype; no clonal chromosomal abnormalities detected. Indication for examination D7510 Secondary polycythemia Note Submicroscopic rearrangements, small structural chromosomal aberrations, DNA-level differences cannot be ruled out with the method used." I am quite confused as JAK2 positivity typically suggests PV, yet the biopsy suggests otherwise, possibly indicating secondary polycythemia. Could you please clarify based on this information what you personally think is more likely, Polycythemia Vera or another secondary cause? Thank you very much for your help.

Male | 67

Your father's symptoms and test results do suggest some complexity. The presence of JAK2 mutation often points towards Polycythemia Vera (PV), but the bone marrow biopsy does not show typical myeloproliferative features, suggesting it might be secondary polycythemia instead. Consult a hematologist, specializing in blood disorders, and can provide a more accurate diagnosis and appropriate treatment plan.

 

Answered on 3rd July '24

Read answer

  1. Home >
  2. Anemia Treatment doctors >
  3. Chennai >
  4. Pammal

Get Free Assistance!

Fill out this form and our health expert will get back to you.