Drug eruption

Examples of drug eruptions. (A) Bullous dermatitis caused by sulfathiazole (B) Fixed drug eruption caused by phenolphtalein (C) Bullous erythema multiforme (D) Diffuse photosensitivity reaction.

In medicine, a drug eruption is an adverse drug reaction of the skin. Most drug-induced cutaneous reactions are mild and disappear when the offending drug is withdrawn.[1] These are called "simple" drug eruptions. However, more serious drug eruptions may be associated with organ injury such as liver or kidney damage and are categorized as "complex".[2] Drugs can also cause hair and nail changes, affect the mucous membranes, or cause itching without outward skin changes.[3]

The use of synthetic pharmaceuticals and biopharmaceuticals in medicine has revolutionized human health, allowing us to live longer lives. Consequently, the average human adult is exposed to many drugs over longer treatment periods throughout a lifetime.[4] This unprecedented rise in pharmaceutical use has led to an increasing number of observed adverse drug reactions.[4]

There are two broad categories of adverse drug reactions. Type A reactions are known side effects of a drug that are largely predictable and are called, pharmatoxicologic.[5] Whereas Type B or hypersensitivity reactions, are often immune-mediated and reproducible with repeated exposure to normal dosages of a given drug.[5] Unlike type A reactions, the mechanism of type B or hypersensitivity drug reactions is not fully elucidated. However, there is a complex interplay between a patient's inherited genetics, the pharmacotoxicology of the drug and the immune response that ultimately give rise to the manifestation of a drug eruption.[5]

Because the manifestation of a drug eruption is complex and highly individual, there are many subfields in medicine that are studying this phenomenon. For example, the field of pharmacogenomics aims to prevent the occurrence of severe adverse drug reactions by analyzing a person's inherited genetic risk.[6] As such, there are clinical examples of inherited genetic alleles that are known to predict drug hypersensitivities and for which diagnostic testing is available.[6]

## Contents

* 1 Classification
* 1.1 By appearance
* 1.2 By mechanism
* 1.3 By drug
* 2 Diagnosis and screening tests
* 3 See also
* 4 References
* 5 External links

## Classification

Some of the most severe and life-threatening examples of drug eruptions are erythema multiforme, Stevens–Johnson syndrome (SJS), toxic epidermal necrolysis (TEN), hypersensitivity vasculitis, drug induced hypersensitivity syndrome (DIHS), erythroderma and acute generalized exanthematous pustulosis (AGEP).[4] These severe cutaneous drug eruptions are categorized as hypersensitivity reactions and are immune-mediated. There are four types of hypersensitivity reactions and many drugs can induce one or more hypersensitivity reactions.[4]

Hypersensitivity Reactions[4] Reaction  | Description  | Mediator  | Mechanism  | Clinical phenotype

|
|
|
|

Type I  | Immediate  | IgE  | antigen binds to mast cell/

basophil surface receptors

| Urticarial (hives), anaphylaxis,

angioedema

TypeII  | Antibody-mediated  | IgM, IgG  | antibody binds antigen leading to

complement-driven cell lysis

| drug-induced thrombocytopenia,

hemolytic anemia, Goodpasture's, ANCA vasculitis

Type III  | Immune complex  | IgM, IgG, IgA  | antigen-antibody complex deposits

in tissues-triggers recruitment of leukocytes

| Serum sickness, Henoch-Schonlein Purpura
Type IV  | Delayed-type  | T-lymphocytes  | Activated T-cells produce cytokines causing

inflammation leading to tissue destruction

| Drug reaction with eosinophilia and systemic symptoms (i.e. DRESS syndrome or DIHS), Stevens–Johnson syndrome, toxic epidermal necrolysis, acute generalized exanthematous pustulosis

### By appearance

The most common type of eruption is a morbilliform (resembling measles) or erythematous rash (approximately 90% of cases).[7] Less commonly, the appearance may also be urticarial, papulosquamous, pustular, purpuric, bullous (with blisters) or lichenoid.[3] Angioedema can also be drug-induced (most notably, by angiotensin converting enzyme inhibitors).

### By mechanism

The underlying mechanism can be immunological (such as in drug allergies) or non-immunological (for example, in photodermatitis or as a side effect of anticoagulants). A fixed drug eruption is the term for a drug eruption that occurs in the same skin area every time the person is exposed to the drug. Eruptions can occur frequently with a certain drug (for example, with phenytoin[8]), or be very rare (for example, Sweet's syndrome following the administration of colony-stimulating factors[9]).

### By drug

The culprit can be both a prescription drug or an over-the-counter medication.

Examples of common drugs causing drug eruptions are antibiotics and other antimicrobial drugs, sulfa drugs, nonsteroidal anti-inflammatory drugs (NSAIDs), biopharmaceuticals, chemotherapy agents, anticonvulsants and psychotropic drugs. Common examples include photodermatitis due to local NSAIDs (such as piroxicam) or due to antibiotics (such as minocycline), fixed drug eruption due to acetaminophen or NSAIDs (Ibuprofen), and the rash following ampicillin in cases of mononucleosis.[2]

Certain drugs are less likely to cause drug eruptions (rates estimated to be ≤3 per 1000 patients exposed). These include: digoxin, aluminum hydroxide, multivitamins, acetaminophen, bisacodyl, aspirin, thiamine, prednisone, atropine, codeine, hydrochlorothiazide, morphine, insulin, warfarin and spironolactone.[2]

## Diagnosis and screening tests

Drug eruptions are diagnosed mainly from the medical history and clinical examination. However, they can mimic various other conditions, thus delaying diagnosis (for example, in drug-induced lupus erythematosus, or the acne-like rash caused by erlotinib). A skin biopsy, blood tests or immunological tests can also be useful.

Drug reactions have characteristic timing. The typical amount of time it takes for a rash to appear after exposure to a drug can help categorize the type of reaction. For example, Acute generalized exanthematous pustulosis usually occurs within 4 days of starting the culprit drug. Drug Reaction with Eosinophilia and Systemic Symptoms usually occurs between 15 and 40 days after exposure. Toxic epidermal necrolysis and Stevens–Johnson syndrome typically occur 7–21 days after exposure. Anaphylaxis occurs within minutes. Simple exanthematous eruptions occur between 4 and 14 days after exposure.[2]

TEN and SJS are severe cutaneous drug reactions that involve the skin and mucous membranes. To accurately diagnose this condition, a detailed drug history is crucial.[4] Often, several drugs may be causative and allergy testing may be helpful.[4] Sulfa drugs are well known to induce TEN or SJS in certain people. For example, HIV patients have an increased incidence of SJS or TEN compared to the general population and have been found to express low levels of the drug metabolizing enzyme responsible for detoxifying sulfa drugs.[5] Genetics plays an important role in predisposing certain populations to TEN and SJS. As such, there are some FDA recommended genetic screening tests available for certain drugs and ethnic populations to prevent the occurrence of a drug eruption.[5] The most well known example is carbamezepine (an anti-convulsant used to treat seizures) hypersensitivity associated with the presence of HLA-B*5801 genetic allele in Asian populations.[6]

Pharmacogenetic alleles associated with cutaneous drug reactions[5] Drug  | Allele  | Population  | Clinical syndrome  | FDA recommended Pharmacogenetic testing

|
|
|
|

Abacavir  | HLA-B*5701  | US European

US African

Australian

| DIHS  | Yes
Allopurinol  | HLA-B*5801  | Han, Korean,

Thai, European

| SJS, TEN, DIHS  | No
Carbamezepine  | HLA-B*1502  | Han, Thai,

Malaysian, Korean

| SJS, TEN  | Yes
Dapsone  | HLA-B*1301  | Chinese  | DIHS  | No
Lamotrigine  | HLA-B*38

HLA-B*1502

| European,

Han

| SJS, TEN  | no recommendation available
Methazolamide  | HLA-B*5901  | Korean  | SJS, TEN  | No
Phenytoin  | HLA-B*1502  | Thai, Han  | SJS, TEN  | Warning

DIHS is a delayed onset drug eruption, often occurring a few weeks to 3 months after initiation of a drug.[2] Worsening of systemic symptoms occurs 3–4 days after cessation of the offending drug.[5] There are genetic risk alleles that are predictive of the development of DIHS for particular drugs and ethnic populations.[5] The most important of which is abacavir (an anti-viral used in the treatment of HIV) hypersensitivity associated with the presence of the HLA-B*5701 allele in European and African population in the United States and Australians.[5]

AGEP is often caused by antimicrobial, anti-fungal or antimalarial drugs.[4] Diagnosis is often carried out by patch testing. This testing should be performed within one month after resolution of the rash and patch test results are interpreted at different time points: 48 hours, 72hours and even later at 96 hours and 120 hours in order to improve the sensitivity.[4]

[10]

## See also

* Fixed drug reaction
* List of cutaneous conditions
* List of human leukocyte antigen alleles associated with cutaneous conditions
* Stevens–Johnson syndrome

## References

1. ↑ Manders SM (June 1995). "Serious and life-threatening drug eruptions". Am Fam Physician 51 (8): 1865–72. PMID 7762478.
2. ↑ 2.0 2.1 2.2 2.3 2.4 Schaffer (2012). Dermatology (3rd ed.). [Philadelphia]: Elsevier Saunders. ISBN 978-0723435716.
3. ↑ 3.0 3.1 "Drug-induced skin, nail and hair disorders". Drug Saf 30 (11): 1011–30. 2007. doi:10.2165/00002018-200730110-00003. PMID 17973540.
4. ↑ 4.0 4.1 4.2 4.3 4.4 4.5 4.6 4.7 4.8 Adverse cutaneous drug eruptions. French, Lars E.. Basel, Switzerland: Karger. 2012. ISBN 9783805599702. OCLC 798579099.
5. ↑ 5.0 5.1 5.2 5.3 5.4 5.5 5.6 5.7 5.8 Dyer, Jon A. (2015). "Immunology of Cutaneous Drug Eruptions" (in en). Cutaneous Drug Eruptions. Springer, London. pp. 3–12. doi:10.1007/978-1-4471-6729-7_1. ISBN 9781447167280.
6. ↑ 6.0 6.1 6.2 Pharmacogenomics : an introduction and clinical perspective. Bertino, Joseph S.. New York: McGraw-Hill. 2013. ISBN 9780071741699. OCLC 793223356.
7. ↑ Bigby, M. (2001-06-01). "Rates of cutaneous reactions to drugs". Archives of Dermatology 137 (6): 765–770. ISSN 0003-987X. PMID 11405768.
8. ↑ Scheinfeld N (August 2003). "Phenytoin in cutaneous medicine: its uses, mechanisms and side effects". Dermatol. Online J. 9 (3): 6. doi:10.5070/D32197W4T4. PMID 12952753. http://dermatology.cdlib.org/93/reviews/dilantin/scheinfeld.html.
9. ↑ Cohen PR (2007). "Sweet's syndrome--a comprehensive review of an acute febrile neutrophilic dermatosis". Orphanet J Rare Dis 2: 34. doi:10.1186/1750-1172-2-34. PMID 17655751.
10. ↑ "Severe adverse cutaneous reactions to drugs". N. Engl. J. Med. 331 (19): 1272–85. November 1994. doi:10.1056/NEJM199411103311906. PMID 7794310.

## External links

Classification|

* ICD-10: L27.0, L27.1
* ICD-9-CM: 692.3, 782.1
* MeSH: D003875

|

External resources|

* eMedicine: derm/104

* v
* t
* e

Hypersensitivity and autoimmune diseases (279.5–6)

Type I/allergy/atopy
(IgE)|

| Foreign|

* Atopic eczema
* Allergic urticaria
* Allergic rhinitis (Hay fever)
* Allergic asthma
* Anaphylaxis
* Food allergy
* common allergies include: Milk
* Egg
* Peanut
* Tree nut
* Seafood
* Soy
* Wheat
* Penicillin allergy

|

Autoimmune|

* Eosinophilic esophagitis

Type II/ADCC

*     * IgM
* IgG

| Foreign|

* Hemolytic disease of the newborn

|

Autoimmune|

| Cytotoxic|

* Autoimmune hemolytic anemia
* Immune thrombocytopenic purpura
* Bullous pemphigoid
* Pemphigus vulgaris
* Rheumatic fever
* Goodpasture syndrome
* Guillain–Barré syndrome

|

"Type V"/receptor|

* Graves' disease
* Myasthenia gravis
* Pernicious anemia

Type III
(Immune complex)|

| Foreign|

* Henoch–Schönlein purpura
* Hypersensitivity vasculitis
* Reactive arthritis
* Farmer's lung
* Post-streptococcal glomerulonephritis
* Serum sickness
* Arthus reaction

|

Autoimmune|

* Systemic lupus erythematosus
* Subacute bacterial endocarditis
* Rheumatoid arthritis

Type IV/cell-mediated
(T cells)|

| Foreign|

* Allergic contact dermatitis
* Mantoux test

|

Autoimmune|

* Diabetes mellitus type 1
* Hashimoto's thyroiditis
* Multiple sclerosis
* Coeliac disease
* Giant-cell arteritis
* Postorgasmic illness syndrome
* Reactive arthritis

GVHD|

* Transfusion-associated graft versus host disease

Unknown/
multiple|

| Foreign|

* Hypersensitivity pneumonitis
* Allergic bronchopulmonary aspergillosis
* Transplant rejection
* Latex allergy (I+IV)

|

Autoimmune|

* Sjögren syndrome
* Autoimmune hepatitis
* Autoimmune polyendocrine syndrome
* APS1
* APS2
* Autoimmune adrenalitis
* Systemic autoimmune disease

* v
* t
* e

Drug reactions (Y40-Y59, E930-E949)

Adverse drug reaction/
drug eruption|

* antibiotics: Penicillin drug reaction
* Sulfonamide hypersensitivity syndrome
* Urticarial erythema multiforme
* Adverse effects of fluoroquinolones

* hormones: Steroid acne
* Steroid folliculitis

* chemotherapy: Chemotherapy-induced acral erythema
* Chemotherapy-induced hyperpigmentation
* Scleroderma-like reaction to taxanes
* Hydroxyurea dermopathy
* Exudative hyponychial dermatitis

* blood: Anticoagulant-induced skin necrosis
* Warfarin necrosis
* Vitamin K reaction
* Texier's disease

* anticonvulsant: Anticonvulsant hypersensitivity syndrome

* water-balance/acid-base: Allopurinol hypersensitivity syndrome

* pulmonary: Leukotriene receptor antagonist-associated Churg–Strauss syndrome

* vaccine: Eczema vaccinatum

* other specified agents: Adverse reaction to biologic agents
* Adverse reaction to cytokines
* Bromoderma
* Halogenoderma
* Iododerma
* Red man syndrome
* Methotrexate-induced papular eruption

* unspecified agent: Acute generalized exanthematous pustulosis
* Bullous drug reaction
* Drug-induced acne
* Drug-induced angioedema
* Drug-related gingival hyperplasia
* Drug-induced lichenoid reaction
* Drug-induced lupus erythematosus
* Drug-induced nail changes
* Drug-induced pigmentation
* Drug-induced pseudolymphoma
* Drug-induced urticaria
* Fixed drug reaction
* Stevens–Johnson syndrome
* Injection site reaction
* Linear IgA bullous dermatosis
* Toxic epidermal necrolysis
* HIV disease-related drug reaction
* Photosensitive drug reaction
* Serum sickness-like reaction

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