Dear Sir, I am taking 1 cobadex czs tab per day. So, you are requested to please let us have the side effect and effect of the same. Regards, Shailendra Kumar

GOOD MORNING SIR,I NAVEEN KUMAR,I AM JUST 25 YEARS OLD.I AM SUFFERING FROM HYPERTENSION FROM 2 MONTHS,I USED STAMLO BETA FOR HYPERTENSION,TWO WEEKS BACK I MET A CARDIOLOGIST,IN THAT TIME MY BP170/100.PREVIOUSLY IT WAS CONTROLLED BY STAMLOBETA.DOCTOR WROTE FOR ECG&ECHO TEST,ECG TELLS THAT 'RBBB.'&ECHO TELLS THAT MILD CONCENTRIC LVH.OTHERWISE NORMAL.DOCTOR PRESCRIBE BP MEDICATIONS CHANGED FROM STAMLO BETA(ATENALOL+AMOLDOPINE)TO METXL-O(METOPROLOL+OLMESARTAN)&SAID THAT NOTHING TO WORRY ,RBBB&MILD CONCENTRIC LVH WILL BE REGRESS.BUT MY BP WAS NOT CONTROLLED ALL THE DAY IT IS RAISED AT NIGHT TIME.TELL ME YOUR SUGGESTION&IS RBBB&LVH REGRESSED,IF WITH CONTROLLED HYPERTENSION?&I HAVE DONE COMPLETE MASTER HEALTH CHECK UP,ALL ARE NORMAL.TELL ME SUGGESTION PLEASE.THANKS®ARDS,NAVEEN KUMAR.

My father had black stools (upon test it had occult blood), they did endoscopy and found an ulcer in lesser curvature. they did sclerotherapy. after couple of days the stools were normal in color. he got discharged. biopsy showed H.pylori and he was given h.pylori kit, orafer xt and cobadex since he had become anemic. after 2 days he fell unconscious, pissed in pants and later passed stools brown again. hospitalized him again. occult blood was present in stools from tests. they did endoscopy and found no bleeding from ulcer where sclerotherpy was done. everything normal in the stomoch and in both duodenum. he is still passing brown stools. donot know why ? please give your opinion.

Name – Biman Das Age – 28 years Indian origin, stays in Bangalore, India. 9th July 2012 - hemoglobin electrophoresis suggestive of Homozygous Hemoglobin E disease Complaint – Weakness since 1year. Hi…. Below are the complete tests I have done two days back….. Blood Urea Nitrogen – 11.00 mg/dl Serum Creatinine – 1 mg/dl Serum Glucose – 94 mg/dl SERUM LIVER FUNCTION TEST Billirubin Total – 1.30 mg/dl Billirubin – direct – 0.30 mg/dl SGOT/AST (P5P, IFCC) – 63.00 IU/ml SGPT/ALT (P5P, IFCC) – 142.00 IU/ml ALP – 74 IU/ml Total protein – 7.80 g/dl Serum Albumin – 4.90 g/dl Serum Globulin – 2.90 g/dl ALB/GLOB Ratio – 1.69 g/dl SERUM TSH (ECLIA) – 6.240 IU/mL COMPLETE BLOOD COUNT WBC – 9300.00 /cu.mm RBC – 6.15 million/cu.mm Hemoglobin – 11.90 g/dl Haemotocrit (PCV) – 37.00 % MCV – 61.00 fL MCH – 19.40 Pg MCHC – 31.30 g/dl Platelet count – 135000.00 /Cu.mm DIFFERENTIAL COUNT Neutrophils – 52 % Lymphocytes – 43 % Monocytes – 3.00 % Eosinophils – 2.00 % ESR – 4.00 /1st hour. PERIPHERAL SMEAR EXAMINATION RBC’s – Show moderate anisopoikilocytosis, are microcytic hypochromic with few eliptocytes, target cells. WBC’s – Leucocytes are normal in total count and distribution Plateletes – Plateletes are reduced. Macroplateletes noted. Impression – Microcytic hypochromic blood picture with thrombocytopenia. (Kindly correlate with serum iron,TIBC, ferritin and Hb variant analysis [To rule out hemoglobinopathy]) OTHER TESTS – Routine Urine analysis – All values are normal ECG – Normal study X-Ray of chest – PA View – Normal Study MY HABBITS – Non veg 3 days a week Beer – 3 days a week( 700ml per day) drinking since 10 years. Smoking – 12 cigarettes per day (Smoking since 10 years). More Anxiety and less physical activities. Last one year I am inside my house, just for half an hour I go outside in the morning. MY HISTORY AND TESTS DONE EARLIER – History of acidity, constipation and digestion. 9th July 2012 - Haemoglobin electrophoresis suggestive of Homozygous Haemoglobin E disease. 16th October 2012 - Ultrasound of liver – Fatty Liver 18th October 2012 – Liver function test – All values are normal 18th October 2012 – Pulmonary test – Normal spirometery 18th October 2012 – Complete Haemoglobin – Haemoglobin 12.5 gm/dl, WBC – normal in number and morphology, RBC – Anicocytosis with microcytic hypochromic erythrocytes, mild polychromasia, elliptocytes and taget cells, platelets- adequate Please let me know is it very serious and also let me know some medicines and diet... Regards Biman Das

Hi, im 36, female, breastfeeding my 8 mos old baby. i have a history of acute pyelonephritis on 2006. Now i think its the same problem suffered from fever, chill, nausea for 3 days... i started to take cotrimoxazole in 3 days but switched to norfloxcin 400 mg but didnt let my baby feed on my breast. I had my urinalysis after 4 days. Result says my wbc/hpf is 8 to 14, mucous thread +, rbc/hpf is 1 - 3, ep cells +, crystals amophous phospates +. My question is what i the interpretation of my result? Should i continue norloxacin 400 mg? How many days 7 or up to 10 days? When can i let my baby breastfeed again? Thank you... --_Anna-

My appendix ruptured 4 days before I went into the hospital for any treatment. Obviously at the time I was very unaware of what it was until after being diagnosed through a very rapid volly of tests and scans, which within hours resulted into surgery. I thought I pulled a muscle or broke/chipped a rib. After I woke from survey the doctor explained my appendix did rupture but luckily, and she quoted to "luckily" in the "chances of winning the lottery" way. she went on to explain that it looked like it ruptured days ago.(I went 4 days of same intense pain levels). She said where it ruptured was "luckily" so close to my colon that the poisonous puss acualy fused my ruptured appendix to the side of my colon which resulted in a, and again I quote, "a miracle bandage", that somewhat sealed most of the deadly toxins that surely would of.."should of" killed me within hours, a few days at best, without immediate care and heavy antibiotics. It was so bad she had to remove part of my colon and needed to make 2 separate incisions. I lay here now after a 2 day after care stay, at my home, with a long drain tube still attached and sucking poison out, a bottle of pain meds which I won't take and refused before surgery also, and a huge bottle of strongest antibiotics prescribable that I must take for at minimum 14 days. I'm a single full time father of 3 girls, twins(almost 14) and a 10yr old. We have no other family, they are what I live for, my strength, my joy, my pride and I litteraly thank god every night for allowing me to care, provide, and have another day together. I never thought I could be more grateful for each day given my past I didn't deserve it. my question is simply this, and thank you for reading, Was I really that close to death? Or is my doctor trumping it up so I'm more conscious about seeing my doc more than once every 5-7 years if that? I will start regular check ups and won't tuff things out to much as a result..BUT COULD I HAVE DIED THAT FAST? THAT EASILY?? please be straight up..no bs..no need to be drawn out.. Thank you for your time! God Bless, The GrateFull DaD