Proportion of participants with at least 50% improvement in QoL: intermediate‐term duration of intervention Symptom score reducing index (SSRI) · patients with chronic spontaneous urticaria
It is very uncertain whether loratadine 10 mg changes proportion of participants with at least 50% improvement in QoL:… compared with mizolastine 10 mg (very low certainty).
1 finding from 1 review
Complete cessation of urticaria: intermediate‐term duration of intervention Global assessment of symptom scores · patients with chronic spontaneous urticaria
Loratadine 10 mg showed no clear difference in complete cessation of urticaria: intermediate‐term duration of… compared with emedastine 2 mg (moderate certainty).
1 finding from 1 review
Good or excellent response: intermediate‐term duration of intervention Global assessment of symptom scores · patients with chronic spontaneous urticaria
Loratadine 10 mg showed no clear difference in good or excellent response: intermediate‐term duration of… compared with emedastine 2 mg (moderate certainty).
1 finding from 1 review
Withdrawals due to adverse events · patients with chronic spontaneous urticaria
Loratadine 10 mg showed no clear difference in adverse events leading to withdrawal: intermediate‐term duration of… compared with emedastine 2 mg (moderate certainty).
1 finding from 1 review
Complete suppression of urticaria: short‐term duration of intervention Global assessment of symptom scores · patients with chronic spontaneous urticaria
Loratadine 10 mg showed no clear difference in complete suppression of urticaria: short‐term duration of… compared with hydroxyzine 25 mg (low certainty).
1 finding from 1 review
Withdrawals due to adverse events · patients with chronic spontaneous urticaria
Cetirizine 10 mg showed no clear difference in adverse events leading to withdrawal compared with hydroxyzine 25 mg (low certainty).
1 finding from 1 review
Withdrawals due to adverse events · patients with chronic spontaneous urticaria
Hydroxyzine 25 mg showed no clear difference in adverse events leading to withdrawal: intermediate‐term duration of… compared with placebo (low certainty).
1 finding from 1 review
Complete suppression of urticaria: short‐term duration of intervention (desloratadine 5 mg) Global assessment of symptom scores · patients with chronic spontaneous urticaria
1 finding from 1 review
Complete suppression of urticaria: short‐term duration of intervention (desloratadine 10 mg) Global assessment of symptom scores · patients with chronic spontaneous urticaria
1 finding from 1 review
Complete suppression of urticaria: short‐term duration of intervention (desloratadine 20 mg) Global assessment of symptom scores · patients with chronic spontaneous urticaria
1 finding from 1 review
Complete suppression of urticaria: intermediate‐term duration of intervention (desloratadine 5 mg) Global assessment of symptom scores · patients with chronic spontaneous urticaria
1 finding from 1 review
Adverse effects requiring withdrawal/discontinuation of study medication · patients with chronic spontaneous urticaria
Desloratadine 5 to 20 mg showed no clear difference in adverse effects leading to withdrawal: intermediate‐term duration of… compared with placebo (low certainty).
1 finding from 1 review
Complete suppression of urticaria: short‐term duration of intervention (levocetirizine 5 mg) Global assessment of symptom scores · patients with chronic spontaneous urticaria
1 finding from 1 review
Complete suppression of urticaria: short‐term duration of intervention (levocetirizine 10 mg) Global assessment of symptom scores · patients with chronic spontaneous urticaria
1 finding from 1 review
Total clearance (at 4 weeks or less) Investigator's assessment · patients with seborrhoeic dermatitis
Calcineurin inhibitor showed no clear difference in total clearance (at 4 weeks or less) Investigator's assessment compared with steroid (low certainty).
1 finding from 1 review
Total clearance (at 4 weeks or less) Investigator's assessment · people with seborrhoeic dermatitis of the scalp or face
Steroid showed no clear difference in total clearance (at 4 weeks or less) Investigator's assessment compared with azole (moderate certainty).
1 finding from 1 review
Total clearance (at 4 weeks or less) Investigator's assessment · patients with seborrhoeic dermatitis
Strong steroid (class III or IV) showed no clear difference in total clearance (at 4 weeks or less) Investigator's assessment compared with mild steroid (class I or II) (moderate certainty).
1 finding from 1 review
Total clearance (more than 4 weeks) Investigator's assessment · patients with seborrhoeic dermatitis
Strong steroid (class III or IV) may leads to lower total clearance (more than 4 weeks) Investigator's assessment compared with mild steroid (class I or II) (low certainty).
1 finding from 1 review
Total clearance Investigator's assessment · patients with seborrhoeic dermatitis
Lithium may leads to higher total clearance Investigator's assessment compared with azole (low certainty).
1 finding from 1 review
Mycological cure · patients with tinea cruris and tinea corporis
1 finding from 1 review