|
Index of reports
> All cases (98)
> Cases with Drug Interaction (11)
Below is the selection of adverse event reports related to Celexa (Citalopram) that includes all cases where reactions include drug interaction.
Adverse event in 83 year old male receiving Celexa (Citalopram)
Reported by a pharmacist from United States on 2007-10-18
Patient: 83 year old male
Adverse reactions / side effects: Blood Creatine Phosphokinase Increased, Fatigue, Drug Interaction, Asthenia, Hepatic Enzyme Increased
Adverse event resulted in: hospitalization
Suspect drug(s):
Zocor
Administration route: Oral
Indication: Blood Cholesterol Increased
Start date: 2005-01-01
End date: 2007-09-06
Celexa
Administration route: Oral
Indication: Depression
Start date: 2007-08-06
End date: 2007-09-06
Celexa
Administration route: Oral
Start date: 2007-08-01
End date: 2007-08-05
Celexa
Administration route: Oral
Indication: Panic Attack
Start date: 2007-08-06
End date: 2007-09-06
Celexa
Administration route: Oral
Start date: 2007-08-01
End date: 2007-08-05
Other drugs received by patient: Plavix; Warfarin; Lorazepam; Imdur; Carvedilol; Potassium Chloride; Omeprazole; Metformin; Furosemide
Adverse event in 83 year old male receiving Celexa (Citalopram)
Reported by a pharmacist from United States on 2007-10-01
Patient: 83 year old male
Adverse reactions / side effects: Blood Creatine Phosphokinase Increased, Fatigue, Alanine Aminotransferase Increased, Aspartate Aminotransferase Increased, Drug Interaction, Asthenia, Hepatic Enzyme Increased
Adverse event resulted in: hospitalization
Suspect drug(s):
Celexa
Dosage: 20 mg qd po
Administration route: Oral
Indication: Depression
Start date: 2007-08-06
End date: 2007-09-06
Celexa
Dosage: 20 mg qd po
Administration route: Oral
Indication: Panic Attack
Start date: 2007-08-06
End date: 2007-09-06
Celexa
Dosage: 10 mg qd po
Administration route: Oral
Indication: Depression
Start date: 2007-08-01
End date: 2007-08-05
Celexa
Dosage: 10 mg qd po
Administration route: Oral
Indication: Panic Attack
Start date: 2007-08-01
End date: 2007-08-05
Simvastatin
Dosage: 80 mg qd po
Administration route: Oral
Indication: Blood Cholesterol Increased
Start date: 2005-01-01
End date: 2007-09-06
Other drugs received by patient: Plavix; Warfarin Sodium; Lorazepam; Imdur; Carvedilol; Potassium Chloride; Omeprazole; Metformin HCL; Furosemide
Adverse event in 49 year old male receiving Celexa (Citalopram)
Reported by a physician from United States on 2007-07-31
Patient: 49 year old male, weighing 73.9 kg (162.6 pounds)
Adverse reactions / side effects: Muscle Rigidity, Abdominal Tenderness, Abdominal Discomfort, Lymphocyte Count Decreased, Back Pain, Restlessness, Drug Withdrawal Syndrome, Respiratory Distress, Delirium, Tremor, Aggression, Respiratory Rate Decreased, Mental Disorder, Neutrophil Count Decreased, Drug Ineffective, Rectal Haemorrhage, Therapeutic Agent Toxicity, Drug Interaction, Mental Status Changes, Hepatomegaly, Frequent Bowel Movements, Fatigue, Overdose, Neck Pain, RED Blood Cell Count Decreased, Thrombocytopenia, Blood Pressure Increased, Haemoglobin Decreased, Anxiety, Haematochezia, Heart Rate Increased, Sinus Tachycardia, Leukopenia
Adverse event resulted in: hospitalization
Suspect drug(s):
Celexa
Indication: Depression
Pegasys
Dosage: 90 mcg sc
Indication: Hepatitis C
Start date: 2006-06-15
End date: 2007-03-01
Pegasys
Dosage: 45 mcg qd sc
Indication: Hepatitis C
Start date: 2007-03-01
Effexor
End date: 2007-04-15
Baclofen
Start date: 2007-04-17
Opiate (Nos)
Wellbutrin
Dosage: 150 mg qd po
Administration route: Oral
Indication: Depression
Start date: 2007-04-17
Voltaren
Indication: Pain
Other drugs received by patient: Azithromycin; Hydrochlorothiazide; Toprol-XL
Adverse event in 49 year old male receiving Celexa (Citalopram)
Reported by a consumer/non-health professional from United States on 2007-07-24
Patient: 49 year old male
Adverse reactions / side effects: Agitation, Movement Disorder, Rectal Haemorrhage, Mental Status Changes, Drug Interaction, Muscle Rigidity, Abdominal Tenderness, Abdominal Discomfort, Fatigue, Hepatomegaly, Neck Pain, RED Blood Cell Count Decreased, Thrombocytopenia, Back Pain, Restlessness, Delirium, Respiratory Distress, Tremor, Aggression, Haematochezia, Anxiety, Haemoglobin Decreased, Diarrhoea, Mental Disorder, Sinus Tachycardia, Leukopenia
Adverse event resulted in: hospitalization
Suspect drug(s):
Wellbutrin
Dosage: 150mg per day
Administration route: Oral
Indication: Depression
Start date: 2007-04-17
Pegasys
Dosage: 45mg per day
Indication: Hepatitis C
Start date: 2006-10-15
End date: 2007-05-11
Effexor
Indication: Drug USE FOR Unknown Indication
Start date: 2006-10-01
End date: 2007-04-15
Celexa
Indication: Depression
Opiate
Baclofen
Indication: Drug USE FOR Unknown Indication
Start date: 2007-04-17
Voltaren
Other drugs received by patient: Zithromax; Hydrochlorothiazide; Toprol-XL; Antibiotic
Adverse event in 49 year old male receiving Celexa (Citalopram)
Reported by a physician from United States on 2007-07-12
Patient: 49 year old male
Adverse reactions / side effects: Rectal Haemorrhage, Drug Interaction, Mental Status Changes, Muscle Rigidity, Drug Toxicity, Frequent Bowel Movements, Fatigue, Overdose, RED Blood Cell Count Decreased, Thrombocytopenia, Incorrect Dose Administered, Drug Withdrawal Syndrome, Respiratory Distress, Delirium, Blood Pressure Diastolic Increased, Aggression, Sinus Tachycardia, Leukopenia
Adverse event resulted in: hospitalization
Suspect drug(s):
Baclofen
Dosage: oral
Administration route: Oral
Indication: Drug USE FOR Unknown Indication
Start date: 2007-04-17
Pegasys
Dosage: 45 mcg, subcutaneous
Indication: Hepatitis C
Start date: 2006-10-15
End date: 2007-05-11
Effexor
Dosage: oral
Administration route: Oral
Indication: Drug USE FOR Unknown Indication
End date: 2007-04-15
Celexa
Dosage: oral
Administration route: Oral
Indication: Depression
Opiate Nos()
Indication: Drug USE FOR Unknown Indication
Wellbutrin
Dosage: oral
Administration route: Oral
Indication: Depression
Start date: 2007-04-17
Other drugs received by patient: Zithromax Z-Pack (Azthromycin); Hydrochlorothiazide; Toprol-XL; Ativan; Benadryl; Cogentin (Benzatorpine Mesilate)
Adverse event in 49 year old male receiving Celexa (Citalopram)
Reported by a health professional (non-physician/pharmacist) from United States on 2007-06-26
Patient: 49 year old male
Adverse reactions / side effects: Agitation, Drug Ineffective, Dyskinesia, Rectal Haemorrhage, Drug Interaction, Mental Status Changes, Prothrombin Time Prolonged, Muscle Rigidity, Frequent Bowel Movements, Overdose, Fatigue, RED Blood Cell Count Decreased, Depression, Thrombocytopenia, White Blood Cell Count Decreased, Blood Pressure Increased, Blood Urea Increased, Restlessness, International Normalised Ratio Increased, Drug Withdrawal Syndrome, Blood Bicarbonate Decreased, Delirium, Respiratory Distress, Aggression, Tremor, Haematochezia, Anxiety, Heart Rate Increased, Mental Disorder, Sinus Tachycardia, Leukopenia
Adverse event resulted in: hospitalization
Suspect drug(s):
Celexa
Indication: Depression
Pegasys
Dosage: 45 mcg sc
Indication: Hepatitis C
Start date: 2006-10-15
End date: 2007-05-11
Baclofen
Start date: 2007-04-17
Opiate (Nos)
Wellbutrin
Dosage: 150 mg qd po
Administration route: Oral
Indication: Depression
Start date: 2007-04-17
Other drugs received by patient: Effexor; Azithromycin; Hydrochlorothiazide; Toprol-XL
Adverse event in 49 year old male receiving Celexa (Citalopram)
Reported by a consumer/non-health professional from United States on 2007-06-20
Patient: 49 year old male
Adverse reactions / side effects: Agitation, Movement Disorder, Rectal Haemorrhage, Drug Interaction, Mental Status Changes, Muscle Rigidity, Fatigue, RED Blood Cell Count Decreased, Thrombocytopenia, Restlessness, Respiratory Distress, Delirium, Tremor, Aggression, Haematochezia, Anxiety, Diarrhoea, Mental Disorder, Sinus Tachycardia, Leukopenia
Adverse event resulted in: hospitalization
Suspect drug(s):
Wellbutrin
Dosage: 150mg per day
Administration route: Oral
Indication: Depression
Start date: 2007-04-17
Pegasys
Dosage: 45mg per day
Indication: Hepatitis C
Start date: 2006-10-15
End date: 2007-05-11
Effexor
Indication: Drug USE FOR Unknown Indication
Start date: 2006-10-01
End date: 2007-04-15
Celexa
Indication: Depression
Opiate
Baclofen
Indication: Drug USE FOR Unknown Indication
Start date: 2007-04-17
Other drugs received by patient: Zithromax; Hydrochlorothiazide; Toprol-XL; Antibiotic
Adverse event in 45 year old male receiving Celexa (Citalopram)
Reported by a physician from United States on 2007-06-12
Patient: 45 year old male
Adverse reactions / side effects: Weight Decreased, Pericardial Effusion, Spinal Compression Fracture, Procedural Complication, Arteriosclerosis, Metastatic Neoplasm, Back Pain, Anaemia, Iatrogenic Injury, Lumbar Vertebral Fracture, Respiratory Distress, Nephrosclerosis, Convulsion, Spleen Disorder, Gastrointestinal Disorder, Pleural Fibrosis, Hepatic Function Abnormal, Body Temperature Increased, Osteoporosis, Pain, Drug Interaction, Multiple Myeloma, Fall, Liver Disorder, Stem Cell Transplant, Drug Toxicity, Pleural Effusion, Bone Disorder, Depression, Myocardial Infarction, RIB Fracture, Protein Urine Present, Pulmonary Amyloidosis, Vomiting, Sternal Fracture, Lung Neoplasm, Cardiac Amyloidosis, Ascites, Pulmonary Fibrosis, Intestinal Haemorrhage, Renal Impairment, Arthralgia, Amyloidosis, Spinal Disorder, Cardiac Arrest, Feeling Abnormal
Adverse event resulted in: death
Suspect drug(s):
Celexa
Dosage: 20 mg qd po
Administration route: Oral
Indication: Depression
Start date: 2001-01-01
End date: 2006-09-03
Zyprexa
Dosage: 5 mg qhs
End date: 2006-09-03
Percocet
Indication: Pain
Start date: 2006-08-23
End date: 2006-09-03
Tylenol W / Codeine NO. 3
Indication: Pain
Start date: 2006-08-24
End date: 2006-09-03
Other drugs received by patient: Gabapentin; Miacalcin (Calciitonin, Salmon); Calcium with Vitamin D; Naprosyn; Bactrim DS (Cotrimoxazole); Ditropan XL; Prilosec; Fluconazole; Acyclovir; Acetaminophen; Interferon Alpha; Zoledronic Acid; Erythropoietin Alfa; Colace (Docusate Sodium); Folic Acid; Multi-Vitamin
Adverse event in 56 year old female receiving Celexa (Citalopram)
Reported by a health professional (non-physician/pharmacist) from Canada on 2007-06-12
Patient: 56 year old female
Adverse reactions / side effects: Agitation, Drug Interaction, Depression, Hallucination
Suspect drug(s):
Celexa
Dosage: 40 mg qd po
Administration route: Oral
Dextromethorphan
Dosage: 22 mg q3hr po
Administration route: Oral
Other drugs received by patient: Acetaminophen; Artificial Saliva (Saliva Substitute); Bisacodyl; Dimenhydrinate; Fentanyl; Sodium Phosphates; Furosemide; Glycopyrrolate; Hydromorphone HCL; Ipratropium Bromide; Lorazepam; Salbutamol; Senokot
Adverse event in 41 year old male receiving Celexa (Citalopram)
Reported by a pharmacist from Canada on 2007-04-26
Patient: 41 year old male
Adverse reactions / side effects: Drug Level Increased, Drug Interaction
Suspect drug(s):
Zetia
Administration route: Oral
Indication: Dyslipidaemia
Start date: 2007-03-16
Cellcept
Trazodone Hydrochloride
Administration route: Oral
Indication: Insomnia
Start date: 2007-03-12
Celexa
Indication: Depression
Start date: 2007-03-12
Theophylline
Administration route: Oral
Indication: Bradycardia
Start date: 2007-03-12
Theophylline
Administration route: Oral
Theophylline
Administration route: Oral
Theophylline
Administration route: Oral
Theophylline
Administration route: Oral
End date: 2007-03-28
Magnesium (Unspecified)
Administration route: Oral
Indication: Hypomagnesaemia
Start date: 2007-03-12
Potassium Chloride
Administration route: Oral
Indication: Hypokalaemia
Start date: 2007-03-12
Other drugs received by patient: Acyclovir; Acyclovir; Lasix; Pantoprazole; Prednisone; Prednisone; Tacrolimus; Nystatin; Nystatin; Clonazepam; Clonazepam; Heparin; Clotrimazole; Colace
Adverse event in 27 year old male receiving Celexa (Citalopram)
Reported by a individual with unspecified qualification from United States on 2007-01-10
Patient: 27 year old male
Adverse reactions / side effects: Restlessness, NO Therapeutic Response, Drug Interaction, Tardive Dyskinesia, Nervousness
Suspect drug(s):
Celexa
Dosage: 40 mg qd po
Administration route: Oral
Indication: Obsessive-Compulsive Disorder
Start date: 2005-02-01
End date: 2005-01-01
Risperdal
Indication: Schizoaffective Disorder
Start date: 2003-12-01
End date: 2005-01-01
Risperdal
Dosage: 37.5 mg im
Indication: Schizoaffective Disorder
Start date: 2003-12-01
End date: 2005-01-01
|
