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Elderly
Congestive heart failure
Liver disease
Hypoalbuminemia
Drugs that interfere with theophylline metabolism:
o Alcohol
o Allopurinol
o Erythromycin
o Azithromycin
o Clarithromycin
o Cimetidine
o Cortisone
o Quinolone antibiotics
Abdominal pain:
o Abdominal cramps
Anorexia
Confusion
Diarrhea
Dizziness
Excessive fatigue
Facial flushing
Shortness of breath
Rapid breathing
Headache
Increased urination
Insomnia
Lightheadedness
Muscle twitching
Nausea
Vomiting
Palpitations
Rapid pulse
Tremor
Loss of consciousness
Seizures
Notify your doctor if you take theophylline and develop any of the following:
Notify your doctor if you take theophylline and develop any of the following:
Aminophylline or theophylline are medicines used to prevent and treat wheezing and
other breathing difficulties caused lung diseases such as asthma.
This is for information only and not for use in the treatment or management of an
actual poison exposure. If you have an exposure, you should call your local
emergency number (such as 911) or the National Poison Control Center at 1-800-222-
1222.
Poisonous Ingredient
Aminophylline
Theophylline
Where Found
Aminophylline
Theophylline (Theo-Dur, Slo-Phyllin, Theolair, Slo-Bid)
Various asthma medications
Symptoms
The major life-threatening events of theophylline intoxication are seizures and heart
rhythm disturbances.
Gastrointestinal
o Increased appetite
o Increased thirst
o Nausea
o Vomiting (possibly with blood)
Heart and blood
o High or low blood pressure
o Irregular heartbeat
o Rapid heart rate
o Pounding heartbeat (palpitations)
Lungs
o Breathing difficulty
Muscles and joints
o Muscle twitching and cramping
Nervous system
o Confusion
o Convulsions
o Dizziness
o Fever
o Hallucinations (thinking something is there, but it's not)
o Headache
o Irritability
o Psychosis
o Restlessness
o Sweating
o Trouble sleeping
Gastrointestinal
o Nausea
o Vomiting
Heart and blood
o Irregular heartbeat
o Low blood pressure
o Rapid heartbeat
o Shock
Lungs
o Rapid, deep breathing
Muscles and joints
o Muscle cramps
o Twitching
Nervous system
o Convulsions
o Irritability
o Tremors
Home Care
Seek immediate medical help. Do NOT make a person throw up unless told to do so
by poison control or a health care professional.
Poison Control
The National Poison Control Center (1-800-222-1222) can be called from anywhere
in the United States. This national hotline number will let you talk to experts in
poisoning. They will give you further instructions.
This is a free and confidential service. All local poison control centers in the United
States use this national number. You should call if you have any questions about
poisoning or poison prevention. It does NOT need to be an emergency. You can call
for any reason, 24 hours a day, 7 days a week.
Activated charcoal
Breathing support (artificial respiration)
Kidney dialysis (in severe cases)
Laxative
Tube through the nose into the stomach to wash out the stomach (gastric lavage)
Outlook (Prognosis)
Convulsions and irregular heartbeats may be difficult to control. Some symptoms may
occur up to 12 hours after the overdose.
Alternative Names
Theophylline overdose; Xanthine overdose
Sessler CN.
PURPOSE: To examine the predisposing factors, clinical and laboratory characteristics, management,
PATIENTS AND METHODS: Toxicology records and hospital charts of consecutive patients with a
serum theophylline concentration (STC) greater than 30 mg/L (167 mumol/L) identified in the
emergency departments (EDS) of a University Medical Center and a Veterans Administration Medical
RESULTS: Ten percent and 2.8% of 5,557 consecutive STCs measured in the EDs over 2 years were
greater than 20 mg/L (111 mumol/L) and greater than 30 mg/L (167 mumol/L), respectively. One
hundred sixteen cases with STC greater than 30 mg/L were identified. Fourteen (12%) and 102 (88%)
were due to acute overdose and chronic overmedication, respectively. Principal predisposing factors
included patient and/or physician dosing errors and conditions or medications that reduce theophylline
clearance. One or more toxic manifestations were present in 109 (94%) cases. Fifty percent of patients
had mild toxicity, 38% had moderate toxicity, and 7% had severe or life-threatening toxicity. Seven (6%)
patients died when STC was still in the toxic range and/or as a result of toxicity. Acute overdose was
associated with higher peak STC (p less than 0.001), younger age (p less than 0.01), and greater
mortality (p less than 0.05) than chronic overmedication. Peak STC correlated significantly with the
severity of toxicity for patients with acute overdose (p less than 0.01) but not for patients with chronic
overmedication. All three patients with acute overdose and fatal toxicity had peak STCs greater than
100 mg/L (555 mumol/L) and fulminant toxicity, whereas the four patients with chronic overmedication
who died during toxicity had peak STCs in the 40 to 60 mg/L (222 to 333 mumol/L) range and most died
of respiratory failure rather than directly from toxicity. Patients with acute overdose who had the delayed
onset of severe or life-threatening toxicity and/or died from toxicity were accurately identified using
previously published criteria for prophylactic charcoal hemoperfusion. In contrast, the predictive value of
the criteria applied to patients with chronic overmedication was poor. Two patients with acute overdose
underwent charcoal hemoperfusion, but died. No patient with chronic overmedication received charcoal
hemoperfusion.
CONCLUSION: Toxic-range STCs are relatively common in the ED population, occur primarily as a
result of patient and physician dosing errors, and cause a broad range of toxic manifestations of varying
severity. Peak STC correlates with the severity of toxicity and outcome for acute overdose but not
chronic overmedication intoxication. Previously published criteria for prophylactic charcoal
hemoperfusion accurately identify patients with acute overdose but not patients with chronic
A case of fatal poisoning caused by theophylline toxicity (serum level 127 μg/ml) is
presented. At external examination, skin blisters on regions exposed to pressure were
distinctive. Histologic examination demonstrated subepidermal bullae with
eosinophilic necrosis of the eccrine sweat gland coil but no epidermal necrosis,
vascular changes, or inflammatory infiltrate. To the authors’ knowledge, this is the
first description of coma blisters in a case of theophylline intoxication.