pharmacy by asim

pharmacy by asim ๐Ÿ‘จโ€โš•๏ธ Love to break down complex medical and pharmacology concepts in simple words.
๐ŸŽฏ Follow us to remain updated with knowledge of medicine & health biology.

๐Ÿงช Metformin + Topiramate Drug Interaction ๐Ÿงช-Topiramate can increase metformin toxicity by inducing non-anion gap, hyperc...
29/06/2025

๐Ÿงช Metformin + Topiramate Drug Interaction ๐Ÿงช

-Topiramate can increase metformin toxicity by inducing non-anion gap, hyperchloremic metabolic acidosis through decreased serum bicarbonate.
- Combined use heightens the risk of metabolic acidosis.
- Close monitoring of renal function, acid-base balance, and bicarbonate levels is recommended.

๐ŸŽฏ ๐—ฌ๐—ผ๐˜‚ ๐—ฐ๐—ฎ๐—ป ๐˜ƒ๐—ถ๐˜€๐—ถ๐˜ ๐—บ๐˜† ๐—ฌ๐—ผ๐˜‚๐—ง๐˜‚๐—ฏ๐—ฒ ๐—ฐ๐—ต๐—ฎ๐—ป๐—ป๐—ฒ๐—น ๐—ณ๐—ผ๐—ฟ ๐—ฎ๐—บ๐—ฎ๐˜‡๐—ถ๐—ป๐—ด ๐—ฐ๐—น๐—ถ๐—ป๐—ถ๐—ฐ๐—ฎ๐—น ๐—ฝ๐—ต๐—ฎ๐—ฟ๐—บ๐—ฎ๐—ฐ๐—ผ๐—น๐—ผ๐—ด๐˜† ๐˜ƒ๐—ถ๐—ฑ๐—ฒ๐—ผ๐˜€: https://youtube.com/

๐Ÿ’Š ๐—›๐˜†๐—ฑ๐—ฟ๐—ผ๐˜…๐˜†๐˜‚๐—ฟ๐—ฒ๐—ฎ ๐—–๐—น๐—ถ๐—ป๐—ถ๐—ฐ๐—ฎ๐—น ๐—ฃ๐—ฒ๐—ฎ๐—ฟ๐—น๐˜€ ๐Ÿ’Š- Hydroxyurea is an oral antimetabolite primarily used for chronic myeloid leukemia (CML)...
27/06/2025

๐Ÿ’Š ๐—›๐˜†๐—ฑ๐—ฟ๐—ผ๐˜…๐˜†๐˜‚๐—ฟ๐—ฒ๐—ฎ ๐—–๐—น๐—ถ๐—ป๐—ถ๐—ฐ๐—ฎ๐—น ๐—ฃ๐—ฒ๐—ฎ๐—ฟ๐—น๐˜€ ๐Ÿ’Š

- Hydroxyurea is an oral antimetabolite primarily used for chronic myeloid leukemia (CML), sickle cell anemia, and essential thrombocythemia.
- It works by inhibiting ribonucleotide reductase, blocking DNA synthesis in rapidly dividing cells.
- Benefits include reducing sickle cell crises by boosting fetal hemoglobin (HbF).
- Common side effects are myelosuppression (anemia, leukopenia), GI upset, and skin ulcers.
- Dosing varies by condition (e.g., 15โ€“35 mg/kg/day for sickle cell, 500โ€“1500 mg/day for CML).
- Requires regular blood monitoring due to toxicity risks.
- Contraindicated in severe bone marrow suppression.

๐ŸŽฏ ๐—ฌ๐—ผ๐˜‚ ๐—ฐ๐—ฎ๐—ป ๐˜ƒ๐—ถ๐˜€๐—ถ๐˜ ๐—บ๐˜† ๐—ฌ๐—ผ๐˜‚๐—ง๐˜‚๐—ฏ๐—ฒ ๐—ฐ๐—ต๐—ฎ๐—ป๐—ป๐—ฒ๐—น ๐—ณ๐—ผ๐—ฟ ๐—ฎ๐—บ๐—ฎ๐˜‡๐—ถ๐—ป๐—ด ๐—ฐ๐—น๐—ถ๐—ป๐—ถ๐—ฐ๐—ฎ๐—น ๐—ฝ๐—ต๐—ฎ๐—ฟ๐—บ๐—ฎ๐—ฐ๐—ผ๐—น๐—ผ๐—ด๐˜† ๐˜ƒ๐—ถ๐—ฑ๐—ฒ๐—ผ๐˜€: https://youtube.com/

๐Ÿ’Š Repaglinide Clinical Pearls ๐Ÿ’Š- Repaglinide is a short-acting meglitinide that stimulates rapid, glucose-dependent insu...
26/06/2025

๐Ÿ’Š Repaglinide Clinical Pearls ๐Ÿ’Š

- Repaglinide is a short-acting meglitinide that stimulates rapid, glucose-dependent insulin secretion by targeting pancreatic ฮฒ-cell Kโ‚โ‚œโ‚š channels.
- Used for Type 2 diabetes, itโ€™s taken 15โ€“30 minutes before meals, offering flexible dosing.
- It has a quick onset (~15โ€“30 min) and short duration (~3โ€“4 hours), reducing hypoglycemia risk compared to sulfonylureas.
- Common side effects include hypoglycemia, GI upset, and weight gain.
- Avoid with CYP3A4/CYP2C8 inhibitors (e.g., gemfibrozil).
- Ideal for postprandial hyperglycemia but requires multiple daily doses.
- Monitor in renal/hepatic impairment.

๐ŸŽฏ check out my detailed video about CLINICAL PHARMACOLOGY of REPAGLINIDE: https://youtu.be/T8R3Pvvjw8A?si=0auSLXhQ7MbxCp2P

repaglinide pharmacology, novonorm pharmacology, antidiabetic drugs pharmacology, pharmacology made easy๐Ÿ’Š Repaglinide is a short-acting meglitinide that sti...

๐Ÿ’Š Aspirin has dose-dependent effects ๐Ÿ’Šโฌ‡๏ธ At low doses (75โ€“100 mg/day)- it works as an antiplatelet by irreversibly inhib...
25/06/2025

๐Ÿ’Š Aspirin has dose-dependent effects ๐Ÿ’Š

โฌ‡๏ธ At low doses (75โ€“100 mg/day)
- it works as an antiplatelet by irreversibly inhibiting COX-1, which reduces thromboxane A2 and prevents platelet aggregation.

โฌ†๏ธ At high doses (โ‰ฅ 3 grams/day)
- it has anti-inflammatory effects by significantly reducing peripheral prostaglandin synthesis.

๐ŸŽฏ ๐—ฌ๐—ผ๐˜‚ ๐—ฐ๐—ฎ๐—ป ๐˜ƒ๐—ถ๐˜€๐—ถ๐˜ ๐—บ๐˜† ๐—ฌ๐—ผ๐˜‚๐—ง๐˜‚๐—ฏ๐—ฒ ๐—ฐ๐—ต๐—ฎ๐—ป๐—ป๐—ฒ๐—น ๐—ณ๐—ผ๐—ฟ ๐—ฎ๐—บ๐—ฎ๐˜‡๐—ถ๐—ป๐—ด ๐—ฐ๐—น๐—ถ๐—ป๐—ถ๐—ฐ๐—ฎ๐—น ๐—ฝ๐—ต๐—ฎ๐—ฟ๐—บ๐—ฎ๐—ฐ๐—ผ๐—น๐—ผ๐—ด๐˜† ๐˜ƒ๐—ถ๐—ฑ๐—ฒ๐—ผ๐˜€: https://youtube.com/

๐Ÿ’Š Nebivolol's Unique Features ๐Ÿ’Š- ฮฒโ‚-Selective with vasodilatory effect- Neutral effects on glucose/lipids- May improve e...
24/06/2025

๐Ÿ’Š Nebivolol's Unique Features ๐Ÿ’Š

- ฮฒโ‚-Selective with vasodilatory effect
- Neutral effects on glucose/lipids
- May improve endothelial dysfunction

๐Ÿ“ Combines ฮฒโ‚-blockade + NO-mediated vasodilation โ†’ preferred in HTN, especially in metabolic syndrome.

๐Ÿ’Š Ethambutol is known to cause optic neuritis (leading to blurred vision, color blindness, or vision loss) as a dose-dep...
22/06/2025

๐Ÿ’Š Ethambutol is known to cause optic neuritis (leading to blurred vision, color blindness, or vision loss) as a dose-dependent side effect.

๐Ÿ’Š Patients on ethambutol should undergo baseline and periodic vision monitoring.

- Thrombolytics (e.g., alteplase, tenecteplase) dissolve clots by activating plasmin. - Used in STEMI, stroke (tPA
19/06/2025

- Thrombolytics (e.g., alteplase, tenecteplase) dissolve clots by activating plasmin.
- Used in STEMI, stroke (tPA

๐Ÿ’Š ๐—•๐—ฒ๐˜๐—ฎ ๐—ฏ๐—น๐—ผ๐—ฐ๐—ธ๐—ฒ๐—ฟ๐˜€ ๐—ฎ๐—ป๐—ฑ ๐—ฆ๐—น๐—ฒ๐—ฒ๐—ฝ ๐—ฑ๐—ถ๐˜€๐˜๐˜‚๐—ฟ๐—ฏ๐—ฎ๐—ป๐—ฐ๐—ฒ ๐Ÿ’Š- Beta-blockers like propranolol can cause vivid, strange, or disturbing dreams b...
16/06/2025

๐Ÿ’Š ๐—•๐—ฒ๐˜๐—ฎ ๐—ฏ๐—น๐—ผ๐—ฐ๐—ธ๐—ฒ๐—ฟ๐˜€ ๐—ฎ๐—ป๐—ฑ ๐—ฆ๐—น๐—ฒ๐—ฒ๐—ฝ ๐—ฑ๐—ถ๐˜€๐˜๐˜‚๐—ฟ๐—ฏ๐—ฎ๐—ป๐—ฐ๐—ฒ ๐Ÿ’Š

- Beta-blockers like propranolol can cause vivid, strange, or disturbing dreams by affecting REM sleep and adrenaline receptors.
- Lipophilic types (e.g., propranolol, metoprolol) are more likely to disrupt dreams.
- Managing side effects includes taking doses earlier, improving sleep hygiene, or switching medications.
- Not everyone experiences this, but consult a doctor if dreams become severely disruptive.

๐Ÿ’Š Levofloxacin injection should be administered for adult and pediatric patients by slow IV infusion over 60 minutes_(25...
14/06/2025

๐Ÿ’Š Levofloxacin injection should be administered for adult and pediatric patients by slow IV infusion over 60 minutes_(250 to 500 mg) and over 90 minutes (for 750 mg).
๐Ÿšจ Due to an increased risk of hypotension , bolus or rapid IV administration should be avoided.

๐Ÿ”Ž In addition, the infusion should not use a solution containing multivalent cations. Adequate hydration is essential to prevent crystalluria.

๐ŸŽฏ PPIs may diminish the therapeutic effect of CLOPIDOGREL, do not use OMEPrazole and ESOMEPrazole while taking clopidogr...
11/06/2025

๐ŸŽฏ PPIs may diminish the therapeutic effect of CLOPIDOGREL, do not use OMEPrazole and ESOMEPrazole while taking clopidogrel.

๐Ÿช€ inhibit enzyme CYP2C19 ---> converts clopidogrel into active form (antiplatelet effect).

๐ŸงŠ RABEprazole or PANToprazole have less risk.

๐ŸŽฏ ๐—ฌ๐—ผ๐˜‚ ๐—ฐ๐—ฎ๐—ป ๐˜ƒ๐—ถ๐˜€๐—ถ๐˜ ๐—บ๐˜† ๐—ฌ๐—ผ๐˜‚๐—ง๐˜‚๐—ฏ๐—ฒ ๐—ฐ๐—ต๐—ฎ๐—ป๐—ป๐—ฒ๐—น ๐—ณ๐—ผ๐—ฟ ๐—ฎ๐—บ๐—ฎ๐˜‡๐—ถ๐—ป๐—ด ๐—ฐ๐—น๐—ถ๐—ป๐—ถ๐—ฐ๐—ฎ๐—น ๐—ฝ๐—ต๐—ฎ๐—ฟ๐—บ๐—ฎ๐—ฐ๐—ผ๐—น๐—ผ๐—ด๐˜† ๐˜ƒ๐—ถ๐—ฑ๐—ฒ๐—ผ๐˜€: https://youtube.com/

๐Ÿ’Š ๐—ก๐—ถ๐—ฎ๐—ฐ๐—ถ๐—ปโ€™๐˜€ ๐—œ๐—บ๐—ฝ๐—ฎ๐—ฐ๐˜ ๐—ผ๐—ป ๐—Ÿ๐—ถ๐—ฝ๐—ถ๐—ฑ๐˜€ ๐Ÿ’Šโœ… Niacin + HMG-CoA Reductase Inhibitors (Statins) โ†’ โฌ‡๏ธ LDL (additive effect)โœ… Niacin + Omeg...
08/06/2025

๐Ÿ’Š ๐—ก๐—ถ๐—ฎ๐—ฐ๐—ถ๐—ปโ€™๐˜€ ๐—œ๐—บ๐—ฝ๐—ฎ๐—ฐ๐˜ ๐—ผ๐—ป ๐—Ÿ๐—ถ๐—ฝ๐—ถ๐—ฑ๐˜€ ๐Ÿ’Š

โœ… Niacin + HMG-CoA Reductase Inhibitors (Statins) โ†’ โฌ‡๏ธ LDL (additive effect)
โœ… Niacin + Omega-3 Fatty Acids โ†’ โฌ‡๏ธ Triglycerides (synergistic reduction)
โœ… Niacin Alone โ†’ โฌ†๏ธ HDL (best pharmacologic HDL booster)

๐Ÿšจ ๐—ž๐—ฒ๐˜† ๐—ก๐—ผ๐˜๐—ฒ๐˜€:
- HDL Increase: Niacin raises HDL by 15โ€“35% (highest among drugs).

- LDL/Triglycerides: Works well in combo therapy but not first-line due to side effects (flushing, hepatotoxicity, hyperglycemia).

- ๐—–๐—น๐—ถ๐—ป๐—ถ๐—ฐ๐—ฎ๐—น ๐—จ๐˜€๐—ฒ: Mostly reserved for statin-intolerant patients or severe mixed dyslipidemia.

๐ŸŽฏ ๐—ฌ๐—ผ๐˜‚ ๐—ฐ๐—ฎ๐—ป ๐˜ƒ๐—ถ๐˜€๐—ถ๐˜ ๐—บ๐˜† ๐—ฌ๐—ผ๐˜‚๐—ง๐˜‚๐—ฏ๐—ฒ ๐—ฐ๐—ต๐—ฎ๐—ป๐—ป๐—ฒ๐—น ๐—ณ๐—ผ๐—ฟ ๐—ฎ๐—บ๐—ฎ๐˜‡๐—ถ๐—ป๐—ด ๐—ฐ๐—น๐—ถ๐—ป๐—ถ๐—ฐ๐—ฎ๐—น ๐—ฝ๐—ต๐—ฎ๐—ฟ๐—บ๐—ฎ๐—ฐ๐—ผ๐—น๐—ผ๐—ด๐˜† ๐˜ƒ๐—ถ๐—ฑ๐—ฒ๐—ผ๐˜€: https://youtube.com/

๐Ÿ’Š Proton pump inhibitors (PPIs) are prodrugs activated by stomach acid in parietal cells. They are mainly metabolized by...
05/06/2025

๐Ÿ’Š Proton pump inhibitors (PPIs) are prodrugs activated by stomach acid in parietal cells. They are mainly metabolized by the liver enzyme CYP2C19, though other P450 enzymes also play a role.

๐Ÿ”ŽMetabolic differences explain why PPI effectiveness varies:
- Asians often have higher PPI bioavailability and may need lower doses.
- Elderly patients also experience increased bioavailability, requiring dose adjustments.

โœ… PPIs are the most potent acid-reducing drugs, though other medications can also decrease stomach acid. Understanding their metabolism helps optimize dosing for different populations.

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