Vitamin C
most data5 sources
Everyone has an opinion on vitamin C, and most of them are too generous. At normal oral doses it does real, small things: shortens colds modestly, supports iron uptake, nudges blood pressure down. Fine. The problem is the megadose and IV claims. Three trials of intravenous vitamin C in critical illness have now landed, and all three showed harm, not benefit. The ceiling for this compound is a lot lower than the marketing suggests.
What it is
Vitamin C is the water-soluble ascorbate your body cannot make and must get from food or supplementation. It works as an antioxidant, supports collagen synthesis, and aids iron uptake from plant foods. The biology is real and well mapped.
The reason the dose conversation matters more here than with most vitamins is pharmacokinetics. Oral absorption saturates: bioavailability is complete at a 200 mg dose but drops at 500 mg and above, and plasma concentration plateaus around 1000 mg daily no matter how much you swallow. Intravenous vitamin C bypasses that plateau entirely, reaching plasma concentrations far higher than any oral regimen can produce. That gap is why IV clinics sell it as a different drug, and why the IV trials matter so much. Higher is not always better.
What the research shows
The oral data is solid and modest. The IV data is now in, and it is bad:
Realistic protocols
For the oral floor, which is what most people should care about: eat your fruit and vegetables, and if you want a supplement, 200 to 500 mg daily is the sweet spot where absorption is still efficient and you are well above deficiency without pushing into kidney-stone territory. Going past 1000 mg daily adds nothing to plasma levels and starts adding urinary oxalate, which is the stone risk.
If you train hard or live under physical stress, the cold-incidence data gets more interesting. Marathon runners, skiers, and soldiers in subarctic conditions saw their cold risk cut roughly in half with regular supplementation. For everyone else, it shortens the cold you catch by less than a day and does not prevent it.
Skip the IV drip. Three trials in critical illness, LOVIT in sepsis, VITaCCA after cardiac arrest, VICTORY in severe burns, all showed harm signals. The evidence does not support routine intravenous vitamin C in sepsis, alone or combined with hydrocortisone and thiamine. The pharmacologic-dose story is over.
Side effects
Oral vitamin C at reasonable doses is very safe. The risks show up at high doses and via IV: