ICI 182,780
Side effects
Options:
Show MedDRA Preferred Terms
Side effect
|
Data for drug
|
Placebo
|
Labels
|
|
1
|
2
|
3
|
Asthenia
|
postmarketing, 5.82% - 27%
|
|
x
|
x
|
x
|
Nausea
|
postmarketing, 9.7% - 26%
|
|
x
|
x
|
x
|
Pain
|
postmarketing, 18.9% - 20.3%
|
|
|
x
|
x
|
Malnutrition
|
17.7% - 18.2%
|
|
x
|
x
|
x
|
Vasodilation
|
postmarketing, 17.3% - 17.7%
|
|
|
x
|
|
Headache
|
postmarketing, 6.68% - 16.8%
|
|
x
|
x
|
x
|
Pharyngitis
|
11.6% - 16.1%
|
|
|
x
|
x
|
Bone pain
|
7.49% - 15.8%
|
|
|
x
|
x
|
Back pain
|
7.48% - 14.4%
|
|
x
|
x
|
x
|
Diarrhoea
|
postmarketing, 12.3% - 12.8%
|
|
x
|
x
|
x
|
Dyspnoea
|
4.43% - 14.9%
|
|
|
x
|
x
|
Vomiting
|
postmarketing, 5.61% - 13%
|
|
x
|
x
|
x
|
Abdominal pain
|
11.6% - 11.8%
|
|
|
x
|
x
|
Constipation
|
3.48% - 12.5%
|
|
|
x
|
x
|
Cough increased
|
10.4%
|
|
|
x
|
x
|
Injection site pain
|
6.6% - 11.6%
|
|
|
x
|
x
|
Oedema peripheral
|
9% - 10.2%
|
|
|
x
|
x
|
Pelvic pain
|
9% - 9.9%
|
|
|
x
|
x
|
Anorexia
|
postmarketing, 3.74% - 10.9%
|
|
x
|
x
|
x
|
Arthralgia
|
7.75% - 8.03%
|
|
|
|
x
|
Insomnia
|
6.9% - 8.5%
|
|
|
x
|
x
|
Rash
|
postmarketing, 7.3% - 8%
|
|
x
|
x
|
x
|
Paraesthesia
|
6.4% - 7.6%
|
|
|
x
|
x
|
Fatigue
|
6.42% - 7.48%
|
|
|
|
x
|
Pain in extremity
|
6.93% - 6.95%
|
|
|
|
x
|
Dizziness
|
6.6% - 6.9%
|
|
|
x
|
x
|
Influenza
|
6.4% - 7.1%
|
|
|
x
|
x
|
Body temperature increased
|
6.4%
|
|
|
x
|
x
|
Depression
|
5.7% - 6.9%
|
|
|
x
|
x
|
Chest pain
|
5% - 7.1%
|
|
|
x
|
x
|
Cough
|
5.26% - 5.35%
|
|
|
|
x
|
Sweating
|
5% - 5.2%
|
|
|
x
|
x
|
Accidental injury
|
4.5% - 5.7%
|
|
|
x
|
x
|
Anaemia
|
4.5% - 5%
|
|
|
x
|
x
|
Arthritis
|
2.8% - 6.1%
|
|
|
x
|
x
|
Anxiety
|
3.8% - 5%
|
|
|
x
|
x
|
Musculoskeletal pain
|
3.21% - 5.54%
|
|
|
|
x
|
Urinary tract infection
|
postmarketing, 3.5% - 6.1%
|
|
x
|
x
|
x
|
Hot flush
|
postmarketing, 5.88% - 6.65%
|
|
x
|
x
|
x
|
Angioedema
|
postmarketing
|
|
|
x
|
x
|
Haemorrhage
|
postmarketing
|
|
|
|
x
|
Hepatitis
|
postmarketing
|
|
|
|
x
|
Hypersensitivity
|
postmarketing
|
|
x
|
x
|
x
|
Inflammation
|
postmarketing
|
|
|
x
|
x
|
Leukopenia
|
postmarketing
|
|
|
|
x
|
Pruritus
|
postmarketing
|
|
|
x
|
|
Urticaria
|
postmarketing
|
|
|
x
|
x
|
Vertigo
|
postmarketing
|
|
|
|
x
|
Hepatic failure
|
postmarketing
|
|
x
|
|
x
|
Injection site reaction
|
postmarketing
|
|
x
|
x
|
x
|
Myalgia
|
postmarketing
|
|
|
|
x
|
Digestion impaired
|
postmarketing
|
|
|
x
|
|
Hepatic enzyme increased
|
postmarketing
|
|
|
x
|
|
Breast cancer stage IV
|
postmarketing
|
|
|
x
|
|
Vaginal haemorrhage
|
postmarketing
|
|
x
|
|
x
|
Breast disorder
|
|
|
x
|
|
|
Vaginal moniliasis
|
|
|
x
|
|
|
Infection
|
|
|
x
|
|
|
Connective tissue disorder
|
|
|
x
|
|
|
Gastrointestinal disorder
|
|
|
x
|
|
|
Hepatitis C
|
|
|
x
|
|
|
Immune system disorder
|
|
|
x
|
|
|
Leukorrhea
|
|
|
x
|
|
|
Nervous system disorder
|
|
|
x
|
|
|
Angiopathy
|
|
|
x
|
|
|
Gamma-glutamyltransferase increased
|
|
|
x
|
|
|
Injection site haemorrhage
|
|
|
x
|
|
|
Unspecified disorder of skin and subcutaneous tissue
|
|
|
x
|
|
|
Hepatobiliary disease
|
|
|
x
|
|
|
Blood bilirubin increased
|
|
|
x
|
|
|
Gastrointestinal symptom NOS
|
|
|
|
|
x
|
Injection site haematoma
|
|
|
x
|
|
|
Infestation NOS
|
|
|
x
|
|
|
Venous thromboembolism
|
|
|
x
|
|
|
Indications
Information about indications was extracted from the indications and usage sections of the labels.
Side effects: | 33 |
Source: | EMA |
---|
Side effects: | 43 |
Source: | Health Canada |
---|
Side effects: | 51 |
Source: | FDA Structured Product Label |
---|
Color scheme:
standard – alternative
|
|
100%
|
|
|
75%
|
|
|
50%
|
|
|
10%
|
|
|
frequent (1% to 100%)
|
|
|
infrequent (0.1% to 1%)
|
|
|
rare (<0.1%)
|
|
|
postmarketing
|
|
|
0%
|
|
|
no frequency information
|
|
|
not found on label
|