Aravind Palraj Profile picture
Aug 9 12 tweets 4 min read Read on X
🧵 Drug Combinations That Can Kill — Interactions You Must Never Miss

We prescribe these daily.
Get the combination wrong → bleeding, rhabdomyolysis, bone marrow suppression, cardiac arrest.

Here are the 10 combinations you must always check for 👇
@DrAkhilX @IhabFathiSulima @CelestinoGutirr @Janetbirdope @DurgaPrasannaM1 @SarahSchaferMD @NeuroSjogrens #MedTwitter #RheumTwitterImage
1) Allopurinol or Febuxostat + Azathioprine or 6-Mercaptopurine
❌ Severe bone marrow suppression (xanthine oxidase inhibition).
✅ Avoid the combination; if unavoidable, drastically reduce azathioprine dose and monitor blood counts closely — but switching is safer. Image
2) Methotrexate + Trimethoprim–Sulfamethoxazole (Co-trimoxazole)
❌ Pancytopenia, mucositis, acute kidney injury.
✅ Use alternatives such as nitrofurantoin or fosfomycin for urinary tract infections. Image
3) Colchicine + CYP3A4 or P-glycoprotein inhibitors (e.g., clarithromycin, verapamil, diltiazem, cyclosporine), especially in chronic kidney disease
❌ Toxicity and rhabdomyolysis, possible multi-organ failure.
✅ Prefer azithromycin; avoid combination or reduce colchicine dose significantly.Image
4) Simvastatin or Lovastatin + Strong CYP3A4 inhibitors (e.g., clarithromycin, ketoconazole, protease inhibitors)
❌ Rhabdomyolysis.
✅ Switch to pravastatin or rosuvastatin, or change the interacting drug. Image
5) Warfarin + Trimethoprim–Sulfamethoxazole, Metronidazole, Azole antifungals, or Fluoroquinolones
❌ International Normalized Ratio (INR) spike → major bleeding.
✅ Reduce warfarin dose pre-emptively and monitor INR early, or choose a safer alternative. Image
6) Apixaban or Rivaroxaban + Strong CYP3A4 or P-glycoprotein inhibitors or inducers (e.g., ketoconazole, ritonavir, rifampicin, carbamazepine, phenytoin)
❌ Bleeding (with inhibitors) or clotting (with inducers).
✅ Avoid combination; change anticoagulant or interacting drug. Image
7) Angiotensin-converting enzyme inhibitor or Angiotensin receptor blocker + Spironolactone + Potassium supplements ± Trimethoprim–Sulfamethoxazole
❌ Dangerous hyperkalemia → arrhythmia (especially in chronic kidney disease or elderly).
✅ Avoid stacking; monitor potassium and creatinine closely; use non-trimethoprim antibiotics if possible.Image
8) Macrolide antibiotics or Fluoroquinolone antibiotics + Other QT-prolonging drugs (e.g., amiodarone, antipsychotics, methadone, tricyclic antidepressants)
❌ Torsades de pointes.
✅ Baseline ECG; avoid combination; consider doxycycline where appropriate. Image
9) Linezolid + Selective serotonin reuptake inhibitors (SSRIs), Serotonin–norepinephrine reuptake inhibitors (SNRIs), Monoamine oxidase inhibitors (MAOIs), or Triptans
❌ Serotonin syndrome.
✅ Hold serotonergic drugs if possible and monitor closely. Image
10) Nitrates (e.g., glyceryl trinitrate) + Phosphodiesterase-5 inhibitors (e.g., sildenafil, tadalafil)
❌ Profound hypotension.
✅ Never co-administer; observe washout periods of at least 24–48 hours depending on the drug. Image
📌 Takeaway
Most interactions are predictable if you know the mechanism.
Look out for:
– CYP3A4 and P-glycoprotein effects
– Bone marrow suppression
– Muscle toxicity
– QT prolongation
– Potassium overload

💬 Share this — it could prevent a catastrophe in your next prescription. Image

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More from @Rheumat_Aravind

Aug 10
🧵 Giant Cell Arteritis — Save a Sight in 5 Minutes

The vision loss is often permanent—and preventable.
A zero-fluff checklist: who to treat before tests, when ultrasound beats biopsy, steroid start & taper, and the traps (normal ESR/CRP, “PMR only,” jaw pain without headache).
@IhabFathiSulima @DrAkhilX @CelestinoGutirr @Janetbirdope @vascuk #MedTwitter #NEETPGImage
Why this matters
•GCA is the most common primary vasculitis >50 years
•~15–20% develop vision loss — often before diagnosis
•Half lose the other eye within days if untreated
•Risk drops almost to zero with prompt steroids Image
Classic presentation
•Age ≥50
•New headache (often temporal)
•Jaw claudication (highly specific)
•Visual blurring / loss
•Scalp tenderness (pain on combing hair)
•± Polymyalgia rheumatica symptoms Image
Read 10 tweets
Aug 10
🧵 C3 vs C4 — What the Pattern Really Means (in 30 seconds)

We order complements all the time.
But the pattern is the diagnosis.
Here’s the fast way to read C3/C4 without overthinking. 👇
@IhabFathiSulima @DrAkhilX @CelestinoGutirr @DurgaPrasannaM1 @SarahSchaferMD @EMJNephrology #MedTwitter #RheumatologyImage
1) Quick primer
•C3 = shared hub (alternative + classical).
•C4 = classical pathway marker (C1q → C4).
Pattern > any single value. Image
2) Both C3 ↓ and C4 ↓ → immune-complex “classical burn”
Think: active SLE, infective endocarditis, serum-sickness/drug IC, mixed cryoglobulinemia.
Next: CH50, anti-dsDNA, C1q binding/anti-C1q, blood cultures if febrile. Image
Read 9 tweets
Aug 10
🧵 CK Can Lie — Catching Myositis When Creatine Kinase Is Normal

Myalgia + weakness.
CK is normal.
Everyone relaxes.
That’s how dangerous myositis gets missed. Let’s fix it. 👇
@IhabFathiSulima @DrAkhilX @CelestinoGutirr #MedTwitter Image
1) First principle
Normal CK ≠ no muscle disease. CK reflects muscle necrosis, not strength. Patchy disease, low muscle mass, or perimysial-predominant injury can keep CK normal. Image
2) When CK is often normal (or only mildly ↑)
•Dermatomyositis (esp. MDA5 phenotype)
•Steroid myopathy (treatment complication, not inflammation)
•Inclusion body myositis (>50 yrs; finger flexors/quads)
•Early/patchy disease, chronic burnt-out myositis Image
Read 12 tweets
Aug 9
🧵 Clues Your “Arthritis” Patient Doesn’t Actually Have RA

Not all swollen joints are rheumatoid arthritis.
Some look identical—but aren’t.
Here’s how to spot RA mimics before the label sticks forever 👇
@IhabFathiSulima @DrAkhilX @SarahSchaferMD @Janetbirdope #MedTwitter #RheumatologyImage
1. It’s asymmetric

RA loves symmetry.
If one side is swollen but the other is fine—think again. Image
2. The wrong joints are involved

RA = MCP, PIP, wrists.
If DIP joints are involved → think OA, psoriatic arthritis.
If only large joints → think reactive, viral, crystal arthritis. Image
Read 8 tweets
Aug 9
🧵 When It’s Not Sepsis – Clues That It’s Actually Autoimmunity

Fever.
Tachycardia.
High CRP.
Looks like sepsis—but cultures stay negative, and antibiotics don’t work.

Let’s break down how to catch autoimmune mimicry of infection—before it’s too late. 👇
@IhabFathiSulima @DrIanWeissman @DrAkhilX @CelestinoGutirr @NeuroSjogrens @SarahSchaferMD @drkeithsiau #MedTwitter #RheumTwitterImage
1. The classic setup:

Patient has:
✅ Fever
✅ High CRP
✅ High neutrophils
✅ Looks toxic

But…
🧪 Cultures are negative
🧫 Antibiotics fail
🧠 Something’s not adding up Image
2. When you should pause:

🚩 No response to antibiotics after 48–72 hrs
🚩 Blood cultures negative
🚩 No source on imaging
🚩 Worsening cytopenias
🚩 Rising liver enzymes or ferritin
🚩 Mental status changes Image
Read 10 tweets
Aug 8
🧵 Thrombocytopenia – Not Always ITP

Low platelets aren’t always immune.
Sometimes they bleed.
Sometimes they clot.
Sometimes they’re screaming for help.

Let’s break down how to approach thrombocytopenia with clarity 👇
@IhabFathiSulima @DrAkhilX @drkeithsiau #MedTwitter #HematologyImage
1. First: Is it even real?

Some low counts are lab errors—not pathology.
Check for:
– Platelet clumps in EDTA
– Smear confirmation
– Citrate sample if unsure Image
2. Bleeding? Clotting? Or neither?

🩸 Bleeding → ITP, marrow failure, DIC
🧱 Clotting + low platelets → APS, TMA, HIT
🧪 No symptoms? Still needs evaluation. Image
Read 9 tweets

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