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Index of reports
> Cases resulting in hospitalization (32)
Below is the selection of adverse event reports related to Celexa (Citalopram) that includes cases resulting in hospitalization.
Reports 1 - 25 of 32 Next >>
Adverse event in 53 year old female receiving Celexa (Citalopram)
Reported by a consumer/non-health professional from United States on 2007-10-30
Patient: 53 year old female
Adverse reactions / side effects: Confusional State, HIP Fracture, Visual Disturbance, Fall, Blood Sodium Decreased
Adverse event resulted in: hospitalization
Suspect drug(s):
Celexa
Dosage: 40 mg qd po
Administration route: Oral
Indication: Depression
Start date: 2005-01-01
End date: 2007-10-02
Celexa
Dosage: 40 mg qd po
Administration route: Oral
Indication: Depression
Start date: 2007-10-22
Morphine
Indication: Pain
Other drugs received by patient: Ultracet (Acetaminophen and Tramadol); Percocet; Trazodone HCL; Seroquel; Restoril; Klonopin; Lidoderm; Depakote; Prednisone TAB; Oxybutynin Chloride; Lovastatin; Protonix; Prilosec; Synthroid; Iron; Colace (Docusate Sodium); Estroven
Adverse event in 20 year old female receiving Celexa (Citalopram)
Reported by a consumer/non-health professional from United States on 2007-10-30
Patient: 20 year old female
Adverse reactions / side effects: Ovarian Cyst
Adverse event resulted in: hospitalization
Suspect drug(s):
Celexa
Dosage: 40 mg qd po
Administration route: Oral
Indication: Anxiety
Start date: 2002-01-01
Celexa
Dosage: 40 mg qd po
Administration route: Oral
Indication: Depression
Start date: 2002-01-01
Adverse event in 27 year old male receiving Celexa (Citalopram)
Reported by a individual with unspecified qualification from United States on 2007-10-24
Patient: 27 year old male, weighing 90.9 kg (200.0 pounds)
Adverse reactions / side effects: Overdose
Adverse event resulted in: life threatening event, hospitalization
Suspect drug(s):
Celexa
Dosage: 20mg once daily po
Administration route: Oral
Indication: Bipolar Disorder
Start date: 2006-10-01
End date: 2007-10-21
Celexa
Dosage: 20mg once daily po
Administration route: Oral
Indication: Depression
Start date: 2006-10-01
End date: 2007-10-21
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):
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
Zocor
Administration route: Oral
Indication: Blood Cholesterol Increased
Start date: 2005-01-01
End date: 2007-09-06
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):
Baclofen
Start date: 2007-04-17
Celexa
Indication: Depression
Effexor
End date: 2007-04-15
Opiate (Nos)
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
Voltaren
Indication: Pain
Wellbutrin
Dosage: 150 mg qd po
Administration route: Oral
Indication: Depression
Start date: 2007-04-17
Other drugs received by patient: Azithromycin; Hydrochlorothiazide; Toprol-XL
Adverse event in 49 year old female receiving Celexa (Citalopram)
Reported by a physician from United States on 2007-07-31
Patient: 49 year old female
Adverse reactions / side effects: Movement Disorder, Dystonia, Arthralgia, Blood Cholesterol Increased, Muscle Spasms
Adverse event resulted in: hospitalization
Suspect drug(s):
Celexa
Dosage: 20 mg qd po
Administration route: Oral
Indication: Depression
Start date: 2004-01-01
End date: 2007-05-08
Celexa
Dosage: 20 mg qd po
Administration route: Oral
Indication: Irritability
Start date: 2004-01-01
End date: 2007-05-08
Vytorin
Indication: Blood Cholesterol Increased
Start date: 2007-04-01
End date: 2007-05-08
Adverse event in 49 year old male receiving Celexa (Citalopram)
Reported by a physician from United States on 2007-07-27
Patient: 49 year old male, weighing 74.0 kg (162.8 pounds)
Adverse reactions / side effects: Movement Disorder, Agitation, Blood Pressure Increased, Back Pain, Restlessness, Mental Status Changes, Drug Withdrawal Syndrome, Muscle Rigidity, Respiratory Distress, Delirium, Aggression, Tremor, Anxiety, Neck Pain, Mental Disorder, Sinus Tachycardia
Adverse event resulted in: hospitalization
Suspect drug(s):
Baclofen
Dosage: unknown
Start date: 2007-04-17
Caffeine
Dosage: about 10 cups
Start date: 2007-04-17
End date: 2007-04-17
Celexa
Dosage: unknown
Indication: Depression
Effexor
Dosage: unknown
End date: 2007-04-15
Nicotine
Dosage: tried to smoke 2 packs in one day
Pegasys
Dosage: 90 mcg, frequency unknown
Indication: Hepatitis C
Start date: 2006-06-15
End date: 2007-03-01
Pegasys
Dosage: 45 mcg, frequency unknown
Start date: 2007-03-01
End date: 2007-05-11
Voltaren
Dosage: unknown
Indication: Pain
Wellbutrin
Administration route: Oral
Indication: Depression
Start date: 2007-04-17
Other drugs received by patient: Azithromycin; Hydrochlorothiazide; Parafon; 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):
Baclofen
Indication: Drug USE FOR Unknown Indication
Start date: 2007-04-17
Celexa
Indication: Depression
Effexor
Indication: Drug USE FOR Unknown Indication
Start date: 2006-10-01
End date: 2007-04-15
Opiate
Pegasys
Dosage: 45mg per day
Indication: Hepatitis C
Start date: 2006-10-15
End date: 2007-05-11
Voltaren
Wellbutrin
Dosage: 150mg per day
Administration route: Oral
Indication: Depression
Start date: 2007-04-17
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
Celexa
Dosage: oral
Administration route: Oral
Indication: Depression
Effexor
Dosage: oral
Administration route: Oral
Indication: Drug USE FOR Unknown Indication
End date: 2007-04-15
Opiate Nos()
Indication: Drug USE FOR Unknown Indication
Pegasys
Dosage: 45 mcg, subcutaneous
Indication: Hepatitis C
Start date: 2006-10-15
End date: 2007-05-11
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 2007-07-06
Patient: 49 year old male, weighing 73.9 kg (162.6 pounds)
Adverse reactions / side effects: Back Pain, Rectal Haemorrhage, Mental Status Changes, Abdominal Pain Upper, Haemoglobin Decreased, Haematochezia, Abdominal Discomfort, Hepatomegaly, Fatigue, Diarrhoea, Neck Pain, RED Blood Cell Count Decreased, Thrombocytopenia, Leukopenia
Adverse event resulted in: hospitalization
Suspect drug(s):
Baclofen
Indication: Drug USE FOR Unknown Indication
Celexa
Indication: Depression
Effexor
Indication: Drug USE FOR Unknown Indication
End date: 2007-04-01
Opiate NOS
Indication: Drug USE FOR Unknown Indication
Pegasys
Indication: Hepatitis C
Start date: 2006-06-01
End date: 2007-03-01
Pegasys
Start date: 2007-03-01
End date: 2007-05-11
Voltaren
Wellbutrin
Administration route: Oral
Indication: Depression
Start date: 2007-04-17
Other drugs received by patient: Zithromax; Hydrochlorothiazide; Toprol-XL; Ativan; Benadryl; Cogentin; Parafon
Adverse event in 16 year old male receiving Celexa (Citalopram)
Reported by a health professional (non-physician/pharmacist) from United States on 2007-07-03
Patient: 16 year old male, weighing 73.9 kg (162.7 pounds)
Adverse reactions / side effects: Poor Quality Sleep, Irritability, Anhedonia, TIC, Homicidal Ideation, Suicidal Ideation
Adverse event resulted in: hospitalization
Suspect drug(s):
Celexa
Indication: Depression
Start date: 2006-05-13
End date: 2006-05-30
Celexa
Indication: Depression
Start date: 2004-02-01
End date: 2006-04-14
Celexa
Dosage: 40 mg qd po
Administration route: Oral
Indication: Depression
Start date: 2006-04-15
End date: 2006-05-12
Zoloft
Dosage: 25 mg qd po
Administration route: Oral
Indication: Depression
Start date: 2006-05-26
End date: 2006-05-29
Zoloft
Indication: Depression
Start date: 2006-05-30
Other drugs received by patient: Clonidine; Klonopin
Adverse event in 86 year old female receiving Celexa (Citalopram)
Reported by a pharmacist from United States on 2007-06-28
Patient: 86 year old female, weighing 53.4 kg (117.5 pounds)
Adverse reactions / side effects: Sedation
Adverse event resulted in: hospitalization
Suspect drug(s):
Celexa
Dosage: 40 mg daily po (duration: recently started)
Administration route: Oral
Indication: Depression
Doxepin HCL
Dosage: 150 mg q8h prn po (duration: recently started)
Administration route: Oral
Indication: Pruritus
Adverse event in 20 year old male receiving Celexa (Citalopram)
Reported by a pharmacist from United States on 2007-06-27
Patient: 20 year old male
Adverse reactions / side effects: Alcohol USE, Confusional State, Grand MAL Convulsion, Vomiting, Balance Disorder, Intentional Overdose, Respiratory Arrest, Serotonin Syndrome
Adverse event resulted in: hospitalization
Suspect drug(s):
Celexa
Dosage: 40 mg daily po
Administration route: Oral
Indication: Anxiety Disorder
Start date: 2007-02-16
End date: 2007-03-01
Celexa
Dosage: 40 mg daily po
Administration route: Oral
Indication: Major Depression
Start date: 2007-02-16
End date: 2007-03-01
Other drugs received by patient: ..
Adverse event in 15 year old female receiving Celexa (Citalopram)
Reported by a health professional (non-physician/pharmacist) from United States on 2007-06-26
Patient: 15 year old female, weighing 73.9 kg (162.6 pounds)
Adverse reactions / side effects: Suicide Attempt, Suicidal Ideation
Adverse event resulted in: hospitalization
Suspect drug(s):
Celexa
Indication: Depression
Start date: 2006-03-09
Flagyl
Indication: Crohn's Disease
Start date: 2005-06-24
Seroquel
Administration route: Oral
Start date: 2006-03-09
Other drugs received by patient: Pentasa; Azathioprine; Amoxicillin; Hyoscyamine ER; Prevacid; Metronidazole; Amitriptyline HCL
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):
Baclofen
Start date: 2007-04-17
Celexa
Indication: Depression
Opiate (Nos)
Pegasys
Dosage: 45 mcg sc
Indication: Hepatitis C
Start date: 2006-10-15
End date: 2007-05-11
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 39 year old female receiving Celexa (Citalopram)
Reported by a pharmacist from United States on 2007-06-25
Patient: 39 year old female, weighing 204.1 kg (449.1 pounds)
Adverse reactions / side effects: Cellulitis, Renal Failure, Muscle Abscess
Adverse event resulted in: hospitalization
Suspect drug(s):
Anesthetics (Nos)
Indication: Anaesthesia
Start date: 2007-04-20
End date: 2007-04-20
Celexa
Dosage: 40 mg qd po
Administration route: Oral
Indication: Depression
End date: 2007-04-01
Other drugs received by patient: Lasix; Prinivil; Catapres; Colace (Docusate Sodium); Pepcid; Percocet; Phenergan; Acetaminophen
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):
Baclofen
Indication: Drug USE FOR Unknown Indication
Start date: 2007-04-17
Celexa
Indication: Depression
Effexor
Indication: Drug USE FOR Unknown Indication
Start date: 2006-10-01
End date: 2007-04-15
Opiate
Pegasys
Dosage: 45mg per day
Indication: Hepatitis C
Start date: 2006-10-15
End date: 2007-05-11
Wellbutrin
Dosage: 150mg per day
Administration route: Oral
Indication: Depression
Start date: 2007-04-17
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 2007-06-20
Patient: 49 year old male
Adverse reactions / side effects: Blood Pressure Increased, Agitation, Movement Disorder, Restlessness, Mental Status Changes, Drug Withdrawal Syndrome, Muscle Rigidity, Delirium, Respiratory Distress, Tremor, Aggression, Anxiety, Mental Disorder, Sinus Tachycardia
Adverse event resulted in: hospitalization
Suspect drug(s):
Baclofen
Dosage: unknown
Start date: 2007-04-17
Bupropion Hydrochloride
Administration route: Oral
Indication: Depression
Start date: 2007-04-17
Caffeine
Dosage: about 10 cups
Start date: 2007-04-17
End date: 2007-04-17
Celexa
Dosage: unknown
Indication: Depression
Effexor
Dosage: unknown
End date: 2007-04-15
Nicotine
Dosage: tried to smoke 2 packs in one day
Pegasys
Dosage: 45 mcg, frequency unknown
Indication: Hepatitis C
Start date: 2006-10-15
End date: 2007-05-11
Other drugs received by patient: Azithromycin; Toprol-XL; Hydrochlorothiazide
Adverse event in 55 year old female receiving Celexa (Citalopram)
Reported by a individual with unspecified qualification from United States on 2007-06-20
Patient: 55 year old female
Adverse reactions / side effects: Ankle Fracture, Fall
Adverse event resulted in: hospitalization
Suspect drug(s):
Celexa
Dosage: 40 mg qd po
Administration route: Oral
Indication: Depression
Start date: 2006-10-04
Unknown Study Medication
Dosage: 300 mg bid po
Administration route: Oral
Indication: Schizophrenia
Start date: 2005-05-13
Other drugs received by patient: Aleve
Adverse event in 49 year old female receiving Celexa (Citalopram)
Reported by a physician from United States on 2007-06-05
Patient: 49 year old female
Adverse reactions / side effects: Movement Disorder, Arthralgia, Dystonia, Blood Cholesterol Increased, Tardive Dyskinesia, Muscle Spasms
Adverse event resulted in: hospitalization
Suspect drug(s):
Celexa
Dosage: 20mg qd po
Administration route: Oral
Indication: Depression
Start date: 2004-01-01
End date: 2007-05-08
Celexa
Dosage: 20mg qd po
Administration route: Oral
Indication: Irritability
Start date: 2004-01-01
End date: 2007-05-08
Vytorin
Indication: Blood Cholesterol Increased
Start date: 2007-04-01
End date: 2007-05-08
Adverse event in 49 year old male receiving Celexa (Citalopram)
Reported by a health professional (non-physician/pharmacist) from United States on 2007-06-01
Patient: 49 year old male
Adverse reactions / side effects: Haematochezia, Fatigue, Diarrhoea, RED Blood Cell Count Decreased, Rectal Haemorrhage, Mental Status Changes, Thrombocytopenia, Leukopenia
Adverse event resulted in: hospitalization
Suspect drug(s):
Baclofen
Indication: Drug USE FOR Unknown Indication
Celexa
Indication: Depression
Effexor
Indication: Drug USE FOR Unknown Indication
End date: 2007-04-01
Opiate NOS
Indication: Drug USE FOR Unknown Indication
Pegasys
Indication: Hepatitis C
Start date: 2006-10-01
End date: 2007-05-11
Wellbutrin
Administration route: Oral
Indication: Depression
Start date: 2007-04-17
Other drugs received by patient: Zithromax; Hydrochlorothiazide; Toprol-XL; Ativan; Benadryl; Cogentin
Adverse event in 39 year old female receiving Celexa (Citalopram)
Reported by a pharmacist from United States on 2007-05-17
Patient: 39 year old female, weighing 200.0 kg (440.0 pounds)
Adverse reactions / side effects: Drug Level Increased, Renal Failure Acute
Adverse event resulted in: hospitalization
Suspect drug(s):
Celexa (Citalopram)
Adverse event in female receiving Celexa (Citalopram)
Reported by a physician from Canada on 2007-05-17
Patient: female
Adverse reactions / side effects: Apgar Score LOW, Drug Exposure During Pregnancy, Meconium in Amniotic Fluid, Somnolence Neonatal, Drug Exposure VIA Breast Milk, Brow Presentation
Adverse event resulted in: hospitalization
Suspect drug(s):
Ativan
Dosage: 1 mg qd transplacental
Start date: 2006-09-27
End date: 2006-11-06
Ativan
Dosage: transmammary
End date: 2007-02-28
Celexa
Dosage: transmammary
End date: 2007-02-28
Zyprexa
Dosage: transplacental
Start date: 2006-12-02
End date: 2007-01-10
Adverse event in 39 year old female receiving Celexa (Citalopram)
Reported by a pharmacist from United States on 2007-05-04
Patient: 39 year old female, weighing 204.1 kg (449.1 pounds)
Adverse reactions / side effects: Renal Failure, Cellulitis, Abscess
Adverse event resulted in: hospitalization
Suspect drug(s):
Celexa (Citalopram)
Other drugs received by patient: Lasix; Prinivil; Catapres; Colace (Docusate Sodium); Pepcid; Percocet; Phenergan; Tylenol
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