smoking
12 interactions related to smoking
smoking + vitamin c
Smoking increases oxidative stress and accelerates the body's turnover of vitamin C, leaving smokers with consistently lower blood and tissue levels of ascorbic acid than non-smokers eating the same diet. Because of this, expert nutrition bodies recommend that people who smoke aim for a higher daily vitamin C intake than non-smokers.
smoking + oral contraceptives
Combining cigarette smoking with combined (estrogen-containing) oral contraceptives raises the risk of heart attack, stroke, and blood clots more than either exposure alone, especially after age 35 and with heavier smoking.
smoking + clozapine
Polycyclic aromatic hydrocarbons in tobacco smoke (not nicotine) strongly induce CYP1A2, the liver enzyme that handles most clozapine metabolism, so smokers tend to have lower clozapine levels and need higher doses. The greater danger is stopping smoking: levels can climb sharply over a few days as the enzyme returns to baseline, risking sedation, seizures, and toxicity unless the dose is reviewed.
smoking + olanzapine
Polycyclic aromatic hydrocarbons in cigarette smoke induce CYP1A2, the main enzyme that breaks down olanzapine, so smokers clear the drug faster and run lower blood levels. When someone quits, levels rise over the following days to weeks and side effects can emerge on a previously stable dose. The effect is driven by combustion products, not nicotine.
smoking + theophylline
Combustion products in tobacco smoke induce the liver enzyme CYP1A2, speeding up how fast the body clears theophylline. Smokers therefore tend to need more theophylline to stay in range, and stopping smoking can reverse this within days and push levels into a toxic range unless the dose is reviewed.
smoking + propranolol
Cigarette smoking induces hepatic metabolism of propranolol (mainly via CYP1A2 and glucuronidation), increasing its clearance and lowering propranolol blood levels in smokers compared with non-smokers. Nicotine also independently raises heart rate, blood pressure, and circulating catecholamines, partly counteracting propranolol's beta-blocking effect. Both effects reverse when a person quits smoking.
smoking + caffeine
Polycyclic aromatic hydrocarbons in tobacco smoke induce CYP1A2, the main liver enzyme that breaks down caffeine, so smokers clear caffeine faster and feel it less. When you quit smoking, that fast clearance fades within a few days and your usual caffeine can build up, contributing to jitters, anxiety, palpitations, and poor sleep that can be mistaken for nicotine withdrawal.
smoking + insulin
Smoking worsens insulin resistance through nicotine-driven catecholamine release, oxidative stress, and inflammation, and slows subcutaneous insulin absorption through vasoconstriction, so people with diabetes who smoke typically need more insulin to reach the same glucose control. Quitting improves insulin sensitivity within days to weeks, so insulin doses often need to come down to avoid hypoglycemia.
smoking + varenicline
Varenicline (Chantix/Champix) is a partial agonist at the alpha4-beta2 nicotinic acetylcholine receptor — the same receptor nicotine targets. It makes smoking less rewarding, so it is started before your quit date and you may keep smoking briefly at first. Combining varenicline with nicotine replacement (patches, gum) can raise quit rates but increases side effects such as nausea, headache, vomiting, and dizziness.
smoking + hrt
Smoking speeds up how the liver breaks down estradiol, lowering circulating estrogen and reducing the effectiveness of oral hormone replacement therapy. It also adds to the blood-clot risk that oral HRT already carries.
smoking + vitamin b12
Cigarette smoke can lower usable vitamin B12 by converting active coenzyme forms to inactive cyanocobalamin and by impairing gastric absorption, creating a low-grade nutritional draw rather than a dangerous reaction.
nicotine + adenosine
Nicotine produces sympathomimetic cardiovascular effects (faster heart rate, higher blood pressure, peripheral vasoconstriction) that can complicate the periprocedural setting in which intravenous adenosine is used for supraventricular tachycardia or pharmacologic cardiac stress testing. Direct interference with adenosine itself is mechanistic and largely shown in animal models; the better-documented antagonist that smokers commonly co-ingest is caffeine.