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Transderm Scop (Scopolamine Transdermal) - Side Effects and Adverse Reactions

 
 



ADVERSE REACTIONS

Clinical Trials Experience

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 clinical practice.

Motion Sickness
In motion sickness clinical studies of Transderm Scōp®, the most frequent adverse reaction was dry mouth. This occurred in about two thirds of patients on drug. A less frequent adverse drug reaction was drowsiness, which occurred in less than one sixth of patients on drug. Transient impairment of eye accommodation, including blurred vision and dilation of the pupils, was also observed.

Post-Operative Nausea and Vomiting
In a total of five clinical studies in which Transderm Scōp® was administered perioperatively to a total of 461 patients where safety was assessed, dry mouth was the most frequently reported adverse drug reaction, which occurred in approximately 29% of patients on drug. Dizziness was reported by approximately 12% of patients on drug. Other adverse drug reactions reported from these studies, with a frequency of ≥3% of patients treated with Transderm Scop and with a frequency higher than placebo were, in descending order: somnolence, urinary retention, agitation/restlessness, visual impairment, confusion, mydriasis and pharyngitis (see Table 6.1).

Table 6.1      PONV: Adverse Drug Reactions in ≥3% of Patients

Transderm Scōp®

(N=461)

Placebo

(N=457)

n

%

n

%

Adverse Drug Reactions

303

65.7

259

56.7

Dry mouth

133

28.9

72

15.8

Dizziness

57

12.4

33

7.2

Somnolence

36

7.8

16

3.5

Urinary Retention

33

7.2

30

6.6

Agitation

28

6.1

20

4.4

Visual Impairment

23

5.0

12

2.6

Confusion

18

3.9

14

3.1

Mydriasis

16

3.5

2

0.4

Pharyngitis

15

3.3

10

2.2

Postmarketing Experience

The following adverse drug reactions, further to those reported from clinical trials, have been identified during postapproval use of Transderm Scōp®. Because these reactions are reported voluntarily from a population of uncertain size, it is not always possible to reliably estimate their frequency or to confirm a definite causal relationship.

In worldwide marketing with Transderm Scōp®, the following adverse drug reactions were reported by body system.
Psychiatric disorders: acute psychosis including: hallucinations disorientation, and paranoia.
Nervous system disorders: headache, amnesia, coordination abnormalities, speech disorder, disturbance in attention, restlessness.
General disorders and administration site conditions: application site burning.
Eye disorders: dry eyes, eye pruritis, angle closure glaucoma, amblyopia, eyelid irritation.
Skin and subcutaneous tissue disorders: rash generalized, skin irritation, erythema.
Renal and urinary disorders: dysuria.
Ear and Labyrinth Disorders: vertigo.

Drug Withdrawal/Post-Removal Symptoms

Symptoms such as dizziness, nausea, vomiting, abdominal cramps, sweating, headache mental confusion, muscle weakness, bradycardia and hypotension may occur following abrupt discontinuation of anticholinergic drugs such as Transderm Scōp®. Similar symptoms, including disturbances of equilibrium, have been reported in some patients following discontinuation of use of the Transderm Scōp® system. These symptoms usually do not appear until 24 hours or more after the patch has been removed. These symptoms can be severe and may require medical intervention. Some symptoms may be related to adaptation from a motion environment to a motion-free environment.

These symptoms can be severe and may require medical intervention.



REPORTS OF SUSPECTED TRANSDERM SCOP SIDE EFFECTS / ADVERSE REACTIONS

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

Possible Transderm Scop side effects / adverse reactions in 42 year old female

Reported by a consumer/non-health professional from United States on 2011-10-07

Patient: 42 year old female weighing 79.4 kg (174.6 pounds)

Reactions: Fatigue, Nausea, Dysuria, Disturbance in Attention, Dizziness, Memory Impairment, Disorientation

Suspect drug(s):
Transderm Scop



Possible Transderm Scop side effects / adverse reactions in 32 year old female

Reported by a consumer/non-health professional from United States on 2011-10-14

Patient: 32 year old female

Reactions: Confusional State, Vomiting, Mydriasis, Hallucination, Visual, Nausea, Heart Rate Increased, Formication, Blindness, Tremor

Suspect drug(s):
Transderm Scop
    Dosage: 1 df, once/single
    Start date: 2011-10-08
    End date: 2011-10-08

Transderm Scop
    Dosage: 1 df, once/single
    Start date: 2011-10-08
    End date: 2011-10-09

Transderm Scop
    Dosage: 1 df, once/single
    Indication: Motion Sickness
    Start date: 2011-10-06
    End date: 2011-10-08



Possible Transderm Scop side effects / adverse reactions in 86 year old female

Reported by a consumer/non-health professional from United States on 2011-10-18

Patient: 86 year old female

Reactions: OFF Label USE, Vomiting, DRY Mouth, Condition Aggravated, Disorientation, Amnesia

Suspect drug(s):
Transderm Scop
    Dosage: 1 df, q72h
    Indication: Dizziness
    Start date: 2011-01-01

Transderm Scop
    Indication: Balance Disorder

Other drugs received by patient: Vitamin B-12; Atacand; Labetalol HCL; Levothyroxine Sodium



See index of all Transderm Scop side effect reports >>

Drug label data at the top of this Page last updated: 2013-04-30

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