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Entocort EC (Budesonide) - Side Effects and Adverse Reactions

 
 



ADVERSE REACTIONS

Because clinical trials are conducted under widely varying conditions, adverse reaction rates observed in the clinical trials of a drug cannot be directly compared to rates in the clinical trials of another drug and may not reflect the rates observed in practice.

The safety of ENTOCORT EC was evaluated in 651 patients in five short-term, active disease state studies. They ranged in age from 17 to 74 (mean 35), 40% were male and 97% were white, 2.6% were ≥65 years of age. Five hundred and twenty patients were treated with ENTOCORT EC 9 mg (total daily dose). In general, ENTOCORT EC was well tolerated in these trials. The most common adverse events reported were headache, respiratory infection, nausea, and symptoms of hypercorticism. Clinical studies have shown that the frequency of glucocorticosteroid-associated adverse events was substantially reduced with ENTOCORT EC capsules compared with prednisolone at therapeutically equivalent doses. Adverse events occurring in ≥ 5% of the patients are listed in Table 2:

Table 2 Adverse Events Occurring in ≥5% of the Patients in any Treated Group

ENTOCORT EC

9 mg

n=520

Placebo

n=107

Prednisolone

40 mg

n=145

Comparator

n=88

Adverse Event

Number (%)

Number (%)

Number (%)

Number (%)

Headache

107 (21)

19 (18)

31 (21)

11 (13)

Respiratory Infection

55 (11)

7 (7)

20 (14)

5 (6)

Nausea

57 (11)

10 (9)

18 (12)

7 (8)

Back Pain

36 (7)

10 (9)

17 (12)

5 (6)

Dyspepsia

31 (6)

4 (4)

17 (12)

3 (3)

Dizziness

38 (7)

5 (5)

18 (12)

5 (6)

Abdominal Pain

32 (6)

18 (17)

6 (4)

10 (11)

Flatulence

30 (6)

6 (6)

12 (8)

5 (6)

Vomiting

29 (6)

6 (6)

6 (4)

6 (7)

Fatigue

25 (5)

8 (7)

11 (8)

0 (0)

Pain

24 (5)

8 (7)

17 (12)

2 (2)

The safety of ENTOCORT EC was evaluated in 233 patients in four long-term clinical trials (52 weeks). A total of 145 patients were treated with ENTOCORT EC 6 mg. A total of 8% of ENTOCORT EC patients discontinued treatment due to adverse events compared with 10% in the placebo group. The adverse event profile in long-term treatment of Crohn’s disease was similar to that of short-term treatment with ENTOCORT EC 9 mg in active Crohn’s disease.

In the long-term clinical trials, the following adverse events occurred in ≥ 5% of the 6 mg ENTOCORT EC patients and are not listed in Table 2 or by body system below: diarrhea (10%); sinusitis (8%); infection viral (6%); and arthralgia (5%).

Adverse events occurring in 520 patients treated with ENTOCORT EC 9 mg (total daily dose) in five short-term, active disease state studies. with an incidence <5% and greater than placebo (n=107) are listed below by body system:

Body as a Whole: asthenia, C-Reactive protein increased, chest pain, dependent edema, face edema, flu-like disorder, malaise; Cardiovascular: hypertension; Central and Peripheral Nervous System: hyperkinesia, paresthesia, tremor, vertigo; Gastrointestinal: anus disorder, Crohn’s disease aggravated, enteritis, epigastric pain, gastrointestinal fistula, glossitis, hemorrhoids, intestinal obstruction, tongue edema, tooth disorder; Hearing and Vestibular: Ear infection-not otherwise specified; Heart Rate and Rhythm: palpitation, tachycardia; Metabolic and Nutritional: hypokalemia, weight increase; Musculoskeletal: arthritis aggravated, cramps, myalgia; Psychiatric: agitation, appetite increased, confusion, insomnia, nervousness, sleep disorder, somnolence; Resistance Mechanism: moniliasis; Reproductive, Female: intermenstrual bleeding, menstrual disorder; Respiratory: bronchitis, dyspnea; Skin and Appendages: acne, alopecia, dermatitis, eczema, skin disorder, sweating increased; Urinary: dysuria, micturition frequency, nocturia; Vascular: flushing; Vision: eye abnormality, vision abnormal; White Blood Cell: leukocytosis

For the 145 patients treated with ENTOCORT EC 6 mg (total daily dose) in long-term studies, the following adverse events that are not included in the list above occurred with an incidence <5% but >2% and greater than for placebo: abscess, amnesia, dizziness, fever, pharynx disorder, purpura, rhinitis, and urinary tract infection.

Glucocorticosteroid Adverse Reactions

Table 3 displays the frequency and incidence of signs/symptoms of hypercorticism by active questioning of patients in short-term clinical trials.

Table 3 Summary and Incidence of Signs/Symptoms of Hypercorticism in Short-Term Studies

ENTOCORT EC 9 mg

n=427

Placebo

n=107

Prednisolone Taper 40 mg

n=145

Signs/Symptom

Number (%)

Number (%)

Number (%)

Acne

63 (15)

14 (13)

33 (23) 1

Bruising Easily

63 (15)

12 (11)

13 (9)

Moon Face

46 (11)

4 (4)

53 (37)

Swollen Ankles

32 (7)

6 (6)

13 (9)

Hirsutism 2

22 (5)

2 (2)

5 (3)

Buffalo Hump

6 (1)

2 (2)

5 (3)

Skin Striae

4 (1)

2 (2)

0 (0)

1 Statistically significantly different from ENTOCORT EC 9 mg
2 Adverse event dictionary included term hair growth increased, local and hair growth increased, general.

Table 4 displays the frequency and incidence of signs/symptoms of hypercorticism by active questioning of patients in long-term clinical trials.

Table 4: Summary and Incidence of Signs/Symptoms of Hypercorticism in Long-Term Studies

ENTOCORT EC 3 mg

n-88

ENTOCORT EC 6 mg

n=145

Placebo

n=143

Signs/Symptom

Number (%)

Number (%)

Number (%)

Bruising Easily

Acne

Moon Face

Hirsutism

Swollen Ankles

Buffalo Hump

Skin Striae

4 (5)

4 (5)

3 (3)

2 (2)

2 (2)

1 (1)

2 (2)

15 (10)

14 (10)

6 (4)

5 (3)

3 (2)

1 (1)

0

5 (4)

3 (2)

0

1 (1)

3 (2)

0

0

The incidence of signs/symptoms of hypercorticism as described above in long-term clinical trials was similar to that seen in the short-term clinical trials.

A randomized, open, parallel-group multicenter safety study specifically compared the effect of ENTOCORT EC (<9 mg/day) and prednisolone (<40 mg/day) on bone mineral density over 2 years when used at doses adjusted to disease severity. Bone mineral density decreased significantly less with ENTOCORT EC than with prednisolone in steroid-naïve patients, whereas no difference could be detected between treatment groups for steroid-dependent patients and previous steroid users. The incidence of treatment-emergent symptoms of hypercorticism was significantly higher with prednisolone treatment.

Postmarketing Experience

The following adverse reactions have been identified during postapproval use of ENTOCORT EC. Because these reactions are reported voluntarily from a population of uncertain size, it is not always possible to reliably estimate their frequency or establish a causal relationship to drug exposure.

Immune System Disorders: Anaphylactic reactions; Nervous System Disorders: Benign intracranial hypertension.



REPORTS OF SUSPECTED ENTOCORT EC SIDE EFFECTS / ADVERSE REACTIONS

Below is a sample of reports where side effects / adverse reactions may be related to Entocort EC. The information is not vetted and should not be considered as verified clinical evidence.

Possible Entocort EC side effects / adverse reactions in 29 year old female

Reported by a health professional (non-physician/pharmacist) from France on 2011-10-05

Patient: 29 year old female

Reactions: Myoclonus, Malaise, Visual Impairment, Hyperreflexia, Altered State of Consciousness

Suspect drug(s):
Entocort EC
    Administration route: Oral
    Indication: Crohn's Disease
    Start date: 2011-09-02
    End date: 2011-09-12

Trimebutine
    Administration route: Oral
    Indication: Crohn's Disease
    Start date: 2011-09-02
    End date: 2011-09-12

Acetaminophen and Tramadol HCL
    Dosage: (37.5+325mg)
    Administration route: Oral
    Indication: Crohn's Disease
    Start date: 2011-09-02
    End date: 2011-09-12

Pantoprazole
    Administration route: Oral
    Indication: Crohn's Disease
    Start date: 2011-09-02
    End date: 2011-09-12

Other drugs received by patient: Potassium Chloride



Possible Entocort EC side effects / adverse reactions in 29 year old female

Reported by a physician from France on 2011-10-05

Patient: 29 year old female

Reactions: Myoclonus, Visual Impairment, Hyperreflexia

Suspect drug(s):
Acetaminophen and Tramadol HCL
    Dosage: 37.5 mg / 325 mg
    Administration route: Oral
    Indication: Crohn's Disease
    Start date: 2011-09-02
    End date: 2011-09-12

Pantoprazole
    Administration route: Oral
    Indication: Crohn's Disease
    Start date: 2011-09-02
    End date: 2011-09-12

Trimebutine
    Administration route: Oral
    Indication: Crohn's Disease
    Start date: 2011-09-02
    End date: 2011-09-12

Entocort EC
    Administration route: Oral
    Indication: Crohn's Disease
    Start date: 2011-09-02
    End date: 2011-09-12

Other drugs received by patient: Potassium Chloride



Possible Entocort EC side effects / adverse reactions in 29 year old female

Reported by a physician from France on 2011-10-12

Patient: 29 year old female

Reactions: Myoclonus, Malaise, Visual Impairment, Hyperreflexia, Altered State of Consciousness

Suspect drug(s):
Entocort EC
    Administration route: Oral
    Indication: Crohn's Disease
    Start date: 2011-09-02
    End date: 2011-09-12

Acetaminophen and Tramadol HCL
    Dosage: 37.5 mg / 325 mg
    Administration route: Oral
    Indication: Crohn's Disease
    Start date: 2011-09-02
    End date: 2011-09-12

Pantoprazole
    Administration route: Oral
    Indication: Crohn's Disease
    Start date: 2011-09-02
    End date: 2011-09-12

Trimebutine
    Administration route: Oral
    Indication: Crohn's Disease
    Start date: 2011-09-02
    End date: 2011-09-12

Other drugs received by patient: Potassium Chloride



See index of all Entocort EC side effect reports >>

Drug label data at the top of this Page last updated: 2009-06-24

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