Summary
Commonly reported side effects of dantrolene include: drowsiness. Continue reading for a comprehensive list of adverse effects.
Applies to dantrolene: oral capsule. Other dosage forms:
- intravenous powder for solution, intravenous powder for suspension
Warning
Oral route (Capsule)
Dantrolene may cause hepatotoxicity, and symptomatic hepatitis (fatal and nonfatal) has been reported at various dose levels. Risk of hepatic injury appears to be greater in patients taking a higher dosage, in females, in patients older than 35 years, and in patients taking additional medication(s). Monitor hepatic function, including frequent determination of SGOT or SGPT, during therapy. Discontinue therapy after 45 days if there is no observable benefit.
Serious side effects of Dantrolene
Along with its needed effects, dantrolene may cause some unwanted effects. Although not all of these side effects may occur, if they do occur they may need medical attention. Serious side effects are very rare when dantrolene is taken for a short time, for example, when it is used for a few days before, during, or after surgery or anesthesia to prevent or treat malignant hyperthermia. However, serious side effects may occur, especially when the medicine is taken for a long time.
Check with your doctor immediately if any of the following side effects occur while taking dantrolene:
Less common
- Bloody or black, tarry stools
- bloody or dark urine
- bluish color changes in skin color
- changes in speech
- chest pain
- confusion
- constipation
- convulsions (seizures)
- decrease in frequency of urination
- decrease in urine volume
- difficult urination
- difficulty in moving
- difficulty in passing urine (dribbling)
- difficulty in swallowing
- fast, pounding, or irregular heartbeat or pulse
- increased frequency of urination
- increased urge to urinate during the night
- joint pain
- light-colored stools
- lightheadedness
- loss of bladder control
- mental depression
- muscle aching or cramping
- muscle pains or stiffness
- muscle spasm or jerking of all extremities
- nausea and vomiting
- pain in lower back
- pain or burning while urinating
- pain, tenderness, or changes in skin color
- painful urination
- severe stomach pain
- shortness of breath
- skin rash, hives, or itching
- slow or troubled breathing
- sudden decrease in amount of urine
- sudden loss of consciousness
- swelling of foot or leg
- swollen joints
- unusual tiredness or weakness
- upper right abdominal pain
- vomiting of blood or material that looks like coffee grounds
- waking to urinate at night
- yellow eyes or skin
Other side effects of Dantrolene
Some side effects of dantrolene may occur that usually do not need medical attention. These side effects may go away during treatment as your body adjusts to the medicine. Also, your health care professional may be able to tell you about ways to prevent or reduce some of these side effects.
Check with your health care professional if any of the following side effects continue or are bothersome or if you have any questions about them:
More common
- Diarrhea
- dizziness
- drowsiness
- general feeling of discomfort or illness
- muscle weakness
Less common
- Abdominal or stomach cramps or discomfort
- abnormal hair growth
- acne-like rash
- blurred or double vision or any change in vision
- change in taste
- chills and fever
- disturbed color perception
- excessive tearing
- halos around lights
- headache
- itching skin
- loss of appetite
- night blindness
- overbright appearance of lights
- redness of skin
- seeing double
- skin rash, encrusted, scaly and oozing
- sleeplessness
- slurring of speech or other speech problems
- sudden decrease in amount of urine
- sweating
- trouble in sleeping
- tunnel vision
- unable to sleep
- unusual nervousness
- weight loss
For Healthcare Professionals
Applies to dantrolene: intravenous powder for injection, oral capsule.
General
The more commonly reported adverse reactions have included loss of grip strength, leg weakness, drowsiness, dizziness, nausea, fatigue, diarrhea, thrombophlebitis, and injection site reactions.[Ref]
Hepatic
Common (1% to 10%): Hepatotoxicity, liver function test abnormalities
Frequency not reported: Jaundice, hepatitis, hepatic dysfunction including fatal hepatic failure[Ref]
Gastrointestinal
Several reports of severe constipation and abdominal distention leading to functional obstruction have been reported. Diarrhea may be severe and may necessitate temporary withdrawal of therapy. If diarrhea recurs, therapy should probably be permanently discontinued.[Ref]
Common (1% to 10%): Dysphagia, nausea, vomiting, abdominal pain
Uncommon (0.1% to 1%): Constipation
Rare (less than 0.1%): Intestinal obstruction
Frequency not reported: Abdominal cramps, anorexia, alteration of taste, gastrointestinal bleeding, gastric irritation, diarrhea[Ref]
Hypersensitivity
Postmarketing reports: Anaphylaxis
Local
Common (1% to 10%): Infusion site pain
Postmarketing reports: Thrombophlebitis and tissue necrosis[Ref]
Dermatologic
Frequency not reported: Abnormal hair growth, acne-like rash, eczematoid eruption, sweating, urticaria, rash, erythema[Ref]
Nervous system
Very common (10% or more): Somnolence (up to 17%), dysphonia (13%)
Common (1% to 10%): Headache, dizziness, seizure, lightheadedness, drooling[Ref]
Psychiatric
Frequency not reported: Mental depression, mental confusion, insomnia, nervousness
Genitourinary
Frequency not reported: Incontinence, increased urinary frequency, urinary retention, hematuria, crystalluria, nocturia, difficult urination and/or urinary retention, difficult erection
Cardiovascular
Very common (10% or more): Flushing
Common (1% to 10%): Pericarditis, atrioventricular block, tachycardia
Uncommon (0.1% to 1%): Exacerbation of preexisting cardiac insufficiency
Frequency not reported: Bradycardia, labile blood pressure, erratic blood pressure, heart failure, phlebitis[Ref]
Respiratory
Common (1% to 10%): Pleural effusion with associated eosinophilia
Rare (0.01% to 0.1%): -or- Rare (less than 0.1%):
Frequency not reported: Feeling of suffocation, respiratory depression, respiratory failure, dyspnea
Postmarketing reports: Pulmonary edema[Ref]
Pulmonary edema has developed during treatment of malignant hyperthermia; the contributory effect of the diluent volume and mannitol in these cases is not known.[Ref]
Musculoskeletal
Common (1% to 10%): Muscular weakness, extremity pain
Frequency not reported: Myalgia, backache[Ref]
Hematologic
Frequency not reported: Aplastic anemia, leukopenia, lymphocytic lymphoma, thrombocytopenia[Ref]
Ocular
Common (1% to 10%): Blurred vision
Frequency not reported: Visual disturbances, diplopia, excessive tearing[Ref]
Other
Common (1% to 10%): Feeling abnormal
Frequency not reported: Chills, fever, general malaise[Ref]
Renal
Frequency not reported: Transient lowering of GFR and renal plasma flow following 8 weeks of oral therapy