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Contraindications and Adverse Reactions

Substance Abuse Problems

Table of Contents

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Disorders and Conditions

NIH Research Data by Substance Abuse Problems

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Food & Drug Reaction

Adverse Reactions

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Cannabinoids

Adverse Reaction Info Specific to Cannabinoids

Adverse Reactions to Drugs & Supplements

Summary

Most of the time, medicines  make our lives better. They reduce aches and pains, fight infections,  and control problems such as high blood pressure or diabetes. But  medicines can also cause unwanted reactions.

One problem is interactions, which may occur between

  • Two drugs, such as aspirin and blood thinners
  • Drugs and food, such as statins and grapefruit
  • Drugs and supplements, such as ginkgo and blood thinners
  • Drugs and diseases, such as aspirin and peptic ulcers

Interactions can change the actions of one or both drugs.   The drugs might not work, or you could get side effects.


Side effects are unwanted effects caused by the drugs.  Most are  mild, such as a stomach aches or drowsiness, and go away after you stop  taking the drug.  Others can be more serious.


Drug allergies are another type of reaction.  They can be mild or  life-threatening.  Skin reactions, such as hives and rashes, are the  most common type. Anaphylaxis, a serious allergic reaction, is more rare.


When you start a new prescription or over-the-counter medication, make sure you understand how to take it correctly.  Know which other medications and foods you need to avoid. Ask your health care provider or pharmacist if you have questions. 

Fruit Juices

MedlinePlus-Dietary Supplements

MedlinePlus-Antioxidants

MedlinePlus-Vitamins

  • Among  all fruit juices, grape fruit juice (GFJ) possesses high interaction  with almost all types of drugs. The juice modifies the body’s way of  metabolizing the medication, affecting the liver’s ability to work the  drug through a person’s system. Taniguchi in 2007 reported a case of  purpura (blood spots, pooling of blood underneath the skin) associated  with the ingestion of cilostazol, aspirin and grapefruit juice in 79  years old man. His purpura disappeared upon cessation of grapefruit  juice, although his medication was not altered. The most probable cause  of his purpura is an increase in the blood level of cilostazol because  of the inhibition of cilostazol metabolism by components of grapefruit  juice; Taniguch.
  • Numerous  reports have documented drug interactions with GFJ that occur via  inhibition of CYP3A enzymes. Furanocoumarins present in GFJ inhibit the  intestinal CYP 3A4 and have been shown to increase the oral  bioavailability of medications that are CYP 3A4 substrates like  Felodipine, midazolam, cyclosporine and raise their concentrations above  toxic levels.
  • GFJ  is generally contraindicated to patients taking psychotropics and it is  advised to inform patients about described interaction. The in vitro  data suggest that compounds present in grapefruit juice are able to  inhibit the P-gp activity modifying the disposition of drugs that are  P-gp substrates such as talinolol. The overall exposure of some drugs  can be increased by more than fivefold when taken with GFJ and increase  the risk of adverse effects.
  • With  new anticonvulsants, serum iron and sodium need to be monitored.  Additionally, users are advised to avoid drinking grape fruit juice  within 1-2 hr(s) of taking these anticonvulsants. Furanocoumarines and  active bioflavonoids present in GFJ are also inhibitors of OATP and when  ingested concomitantly, can reduce the oral bioavailability of the OATP  substrate, fexofenadine. Overall, a series of flavonoids present in GFJ  are identified as esterase inhibitors, of which kaempferol and  naringenin are shown to mediate pharmacokinetic drug interaction with  most of the calcium channel antagonist and the statin groups of drugs  such as enalapril and lovastatin due to their capability of esterase  inhibition.
  • Cholesterol-lowering  agent lovastatin should be taken with food to enhance gastrointestinal  absorption and bioavailability. The absorption of rosuvastatin, another  anti-hyper lipidemic agent, was significantly decreased in the fed state  compared with the fasting state, which suggests that rosuvastatin  should be administered on an empty stomach.
  • Simvastatin,  Ezetimibe, pravastatin and fluvastatin may be taken without regards to  food. However, high fiber diets may lower the efficacy of these drugs.  Concomitant administration of statins with food may alter statin  pharmacokinetics or pharmacodynamics, increasing the risk of adverse  reactions such as myopathy or rhabdomyolysis or reducing their  pharmacological action. Consumption of pectin or oat bran together with  Lovastatin reduces absorption of the drug, while alcohol intake does not  appear to affect the efficacy and safety of Fluvastatin treatment.

Find out more - NIH

Monoamnine Oxidases

MedlinePlus-Antidepressants

  • Antidepressant  activity of monoamine oxidase inhibitors (MAOIs) was initially noted in  the 1950s. Although older monoamine oxidase inhibitors (MAOIs) are  effective in the treatment of depressive disorders, they are  under-utilized in clinical practice due to main concerns about  interaction with tyramine-containing food (matured cheese, red vine,  ripped bananas, yogurt, shrimp paste and salami) or so called cheese  reaction, since they are capable of producing hypertensive crisis in  patients taking MAOIs.
  • The  first-generation MAOIs such as phenelzine and isocarboxazid were  largely nonselective inhibitors of both subtypes of MAO, MAO (A) and MAO  (B). These medications carried with them dietary restrictions. Tyramine  is an indirectly acting sympathomimetic agent, is degraded by MAO but  in the presence of MAOIs, it escapes degradation and reaches the  systemic circulation where it is taken up by the adrenergic neuron,  leading to a hypertensive crisis. However, MAOIs have been well  established as an effective intervention for people with  treatment-resistant depression, and transdermal formulations may provide  a valuable therapeutic option and eliminate the drug-food interaction.

Find out more - NIH

Antihypertensive Drugs

MedlinePlus-Blood Pressure Medicines

  • Patients  placed on anti hypertensive drugs will benefit from concomitant  moderate sodium restricted diets. Propranolol serum levels may be  increased if taken with rich protein food. A change in diet from high  carbohydrates/low protein to low carbohydrate/high protein may result in  increased oral clearance. Smoking may decrease its plasma levels of by  increasing its metabolism. The intestinal absorption of celiprolol  (beta-blocker) is inhibited when it is taken with orange juice.  Hesperidin, present in orange juice, is responsible for the decreased  absorption of celiprolol. The absorption of ACEs inhibitors is increased  when taken on an empty stomach. While GFJ increases the bioavailability  of felodipine (Ca2 channel blocker).
  • Licorice  extract, a common ingredient of dietary supplement contains  glycyrrhizin and glycyrrhetinic acid. It is a potent inhibitor of 11-  bet- hydroxyl steroid dehydrogenase, it increases excess of cortisol to  mineralocorticoid receptors causing sodium retention and potassium  depletion, so it may interfere with various medicines including  antihypertensive and antiarrhythmic agents. A high intake of liquorice  can cause hypermineralocorticoidism with sodium retention and potassium  loss, oedema, increased blood pressure and depression of the  renin-angiotensin-aldosterone system. Studies showed that a daily  consumption of glycyrrhizic acid of 95 mg or more caused an increase in  blood pressure. A practical guideline for an acceptable daily intake of  glycyrrhizic acid seems to be 9.5 mg a day. This means no more than  10-30g liquorice and no more than half a cup of liquorice tea a day.

Find out more - NIH

Antibiotics

MedlinePlus-Antibiotics

  • Antibiotics  are widely prescribed in medical practice. Many of them induce or are  subject to interactions that may diminish their anti-infectious  efficiency or elicit toxic effects. Food intake can influence the  effectiveness of an antibiotic.  Avoid co-administration of antibiotics  with milk products which are rich sources of divalent ions, such as  calcium and magnesium that complex with some antibiotics and prevent  their absorption. The intake of dairy products, however, needs to be  monitored and encouraged with appropriate consideration of specific  antibiotics involved.
  • A  number of studies give evidence that fluoroquinolones forming slightly  soluble complex with metal ions of food show reduced bioavailability.  Casein and calcium present in milk decrease the absorption of  ciprofloxacin. The effect of interaction of five fruit juices on the  dissolution and absorption profiles of ciprofloxacin tablets were  determined. It was found that the absorption of ciprofloxacin (500 mg)  tablets can be reduced by concomitant ingestion of the GFJ. Therefore,  to avoid drug therapeutic failures and subsequent bacterial resistance  as a result of sub-therapeutic level of the drug in the systemic  circulation, ingestion of the juice with ciprofloxacin should be  discouraged. Azithromycin absorption is decreased when taken with food,  resulting in a 43% reduction in bioavailability. Tetracycline should be  taken one hour before or two hours after meals, and not taken with milk  because it binds calcium and iron, forming insoluble chelates, and  influencing its bioavailability. The effect of milk added to coffee or  black tea on the bioavailability of tetracycline was evaluated in  healthy individuals. Results showed that even a little quantity of milk  containing extremely small amounts of calcium severely impair the  absorption of the drug, so that the presence of this metal ion should be  carefully controlled in order to avoid decreasing the available  tetracycline.
  • Food-drug  interactions may reduce the bioavailability of drugs taken after meals  (negative food effects). However, enteric-coated tablets that start to  disintegrate when they reach the middle-to-lower region of the small  intestine could reduce negative food effects. Results indicated that  food-drug interactions were avoided by separating the main absorption  site of drugs from that of food components.

Find out more - NIH

Analgesics and Antipyretics (Pain Reliever)

MedlinePlus-Pain Relievers

  • Analgesics  and antipyretics are used to treat mild to moderate pain and fever. For  rapid relief, acetaminophen should be taken in an empty stomach because  food may slow the body absorption of acetaminophen. Co-administration  of acetaminophen with pectin delays its absorption and onset. NSAIDs  like ibuprofen, naproxen, ketoprofen and others can cause stomach  irritation and thus they should be taken with food or milk. Avoid or  limit the use of alcohol because chronic alcohol use can increase the  risk of liver damage or stomach bleeding. The absorption of ibuprofen  and oxycodone when given in the combination tablet was affected by the  concomitant ingestion of food.
  • The  Cmax and AUC0-alpha of ibuprofen were significantly increased after  single and multiple doses of Coca-Cola, thereby indicating increased  extent of absorption of ibuprofen. The daily dosage and frequency of  ibuprofen must be reduced when administered with Coca-Cola. Food intake  did not appear to affect the extent of absorption (ie, total exposure)  of oral Diclofenac potassium soft gelatin capsule at doses.

Find out more - NIH

Cannabinoids

U.S. National Library of Medicine - PubMed Center

PubMed  Central® (PMC) is a free full-text archive of biomedical and life  sciences journal literature at the U.S. National Institutes of Health's  National Library of Medicine (NIH/NLM). In keeping with NLM’s  legislative mandate to collect and preserve the biomedical literature,  PMC serves as a digital counterpart to NLM’s extensive print journal  collection.  PMC was developed and is managed by NLM’s National Center  for Biotechnology Information (NCBI).  PMC makes all content free to  read (in some cases, following an embargo period), as NLM believes that  the best way to ensure the accessibility and viability of digital  material over time is through consistent and active use of the archive.  

Read Studies and Findings

Cannabinoid Related - FDA Recalls, Market Withdrawals and Safety Alerts

The  list below provides information gathered from press releases and  other  public notices about certain recalls of FDA-regulated products.  Not  all recalls have press releases or are posted on this page. Certain  product recalls sometimes merit expanded coverage due to the impact they  have on public health. This section includes details of FDA's  involvement in investigating recalls, a means to search recalled  products, and information for consumers and industry representatives.  

Read Studies and Findings

U.S. National Institutes of Health - MedlinePlus

MedlinePlus  is a service of the National Library of Medicine (NLM),  the world's  largest medical library, which is part of the National  Institutes of  Health (NIH).  Their mission is to present  high-quality, relevant  health and wellness information that is trusted,  easy to understand,  and free of advertising 

Read Studies and Findings

National Center for Complementary and Integrative Health

The National Center for Complementary and Integrative Health  (NCCIH) part of the National Institutes of Health, is the Federal  Government’s lead agency for scientific research on the diverse medical  and health care systems, practices, and products that are not generally  considered part of conventional medicine. NCCIH was formerly known as  the National Center for Complementary and Alternative Medicine. 

Read Studies and Findings

Substance Abuse Problems

  • Alcohol 
  • Alcohol Abuse see Alcohol Use Disorder (AUD) 
  • Alcohol Abuse in Pregnancy see Pregnancy and Drug Use 
  • Alcohol and Youth see Underage Drinking 
  • Alcohol Consumption see Alcohol 
  • Alcohol Dependence see Alcohol Use Disorder (AUD) 
  • Alcohol Use Disorder (AUD) 
  • Alcohol Use Disorder (AUD) Treatment 
  • Alcohol      Withdrawal see Alcohol Use Disorder (AUD) 
  • Alcoholism      see Alcohol Use Disorder (AUD) 
  • Amphetamines      see Club Drugs; Methamphetamine 
  • Anabolic Steroids 
  • Binge Drinking see Alcohol Use Disorder (AUD) 
  • Cannabis see Marijuana 
  • Chewing Tobacco see Smokeless Tobacco 
  • Club Drugs 
  • Cocaine 
  • Crack see Cocaine 
  • Dip see Smokeless Tobacco 
  • Drinking see Alcohol; Alcohol Use Disorder (AUD) 
  • Drug abuse see Drug Use and Addiction 
  • Drug Abuse in Pregnancy see Pregnancy and Drug Use 
  • Drug  Abuse, Prescription see Prescription Drug Misuse 
  • Drug Use and Addiction 
  • Drugs and Young People 
  • Dual Diagnosis 

Top

  • E-Cigarettes 
  • Ecstasy see Club Drugs 
  • FAS see Fetal Alcohol Spectrum Disorders 
  • Fetal Alcohol Spectrum Disorders 
  • Fetal Alcohol Syndrome see Fetal Alcohol Spectrum Disorders 
  • GHB see Club Drugs 
  • Hallucinogens see Club Drugs; Drug Use and Addiction 
  • Heroin 
  • Huffing see Inhalants 
  • Inhalants 
  • Marijuana 
  • MDMA see Club Drugs 
  • Methamphetamine 
  • Nicotine see Smoking 
  • Opiates see Heroin; Opioid Misuse and Addiction 
  • Opioid Abuse and Addiction see Opioid Misuse and Addiction 
  • Opioid Abuse and Addiction Treatment see Opioid Misuse and Addiction Treatment 
  • Opioid Misuse and Addiction 
  • Opioid Misuse and Addiction Treatment 
  • Opioid Overdose 
  • Oral Tobacco see Smokeless Tobacco 
  • Performance-Enhancing Drugs see Anabolic Steroids 
  • Pregnancy and Drug Use 
  • Pregnancy and Opioids 
  • Pregnancy and Substance Abuse see Pregnancy and Drug Use 
  • Prescription Drug Abuse see Prescription Drug Misuse 
  • Prescription Drug Misuse 

Top

  • Quitting Smoking 
  • Rohypnol see Club Drugs 
  • Safe Opioid Use 
  • Smokeless Tobacco 
  • Smoking 
  • Smoking and Youth 
  • Smoking Cessation see Quitting Smoking 
  • Smoking in Pregnancy see Pregnancy and Drug Use 
  • Snuff see Smokeless Tobacco 
  • Spit Tobacco see Smokeless Tobacco 
  • Steroids,  Anabolic see Anabolic Steroids 
  • Substance Abuse see Alcohol Use Disorder (AUD); Drug Use and Addiction; Drugs and Young People 
  • Substance Abuse in Pregnancy see Pregnancy and Drug Use 
  • Teen Drug Abuse see Drugs and Young People 
  • Teen Smoking see Smoking and Youth 
  • Teenage Drinking see Underage Drinking 
  • Tobacco Smoking see Smoking 
  • Tobacco, Smokeless see Smokeless Tobacco 
  • Underage Drinking 
  • Vaping see E-Cigarettes 

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