REPORTS OF SIDE EFFECTS / ADVERSE REACTIONS RELATED TO COGENTIN
Below is a sample of reports where side effects / adverse reactions may be related to Cogentin. The information is not vetted and should not be cosidered as verified clinical evidence.
Possible Cogentin side effects / adverse reactions in 48 year old male
Reported by a physician from United States on 2007-02-20
Patient: 48 year old male
Reactions: RED Cell Distribution Width Increased, Thrombocythaemia
Suspect drug(s):
Cogentin
Indication: Drug USE FOR Unknown Indication
Risperidone
Dosage: q2w; im
Indication: Drug USE FOR Unknown Indication
Depakote
Indication: Drug USE FOR Unknown Indication
Possible Cogentin side effects / adverse reactions in 27 year old female
Reported by a individual with unspecified qualification from United States on 2007-03-20
Patient: 27 year old female weighing 77.1 kg (169.6 pounds)
Reactions: Weight Increased, Stomatitis, Visual Disturbance, Tardive Dyskinesia
Suspect drug(s):
Risperdal
Dosage: 25-55 millagrams ever 2 weeks iv
Indication: Schizophrenia
Start date: 2006-07-01
End date: 2007-01-31
Cogentin
Dosage: 3 a day 3 a day po
Administration route: Oral
Indication: Restlessness
Start date: 2006-07-01
End date: 2006-09-01
Possible Cogentin side effects / adverse reactions in 95 year old female
Reported by a pharmacist from United States on 2007-05-30
Patient: 95 year old female weighing 56.9 kg (125.2 pounds)
Reactions: Confusional State, Speech Disorder, Dystonia, Agonal Death Struggle, Motor Dysfunction, Chest Pain, Respiratory Arrest, Extrapyramidal Disorder, Respiratory Distress, Muscle Spasms
Adverse event resulted in: death, hospitalization
Suspect drug(s):
Ranexa
Dosage: 1000 mg bid po
Administration route: Oral
Indication: Angina Pectoris
Start date: 2007-05-25
End date: 2007-05-28
Ranexa
Dosage: 1000 mg bid po
Administration route: Oral
Indication: Coronary Artery Disease
Start date: 2007-05-25
End date: 2007-05-28
Cogentin
Dosage: 1 mg once iv
Indication: Extrapyramidal Disorder
Start date: 2007-05-29
End date: 2007-05-29
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