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This is an index of reports of adverse events (side effects, adverse reactions, etc.) related to Celexa (Citalopram). Click on the relevant link below to view a selection of reports according to the event's seriousness level and/or the nature of the side effect / adverse reaction. Or scroll down to view a sample of recent reports further on this page.
Our database includes reports from Jan 2007 to Dec 2007. The information is not vetted and should not be cosidered as verified clinical evidence.
All cases (98)
Cases resulting in a serious event (87)
Cases resulting in death (16)
Cases resulting in life threatening events (4)
Cases resulting in hospitalization (32)
Cases resulting in other serious reactions (47)
Below is a sample of reports where side effects / adverse reactions may be related to Celexa (Citalopram). For a complete list and/or a specific selection of reports, please use the links in the index above.
Adverse event in receiving Celexa (Citalopram)
Reported by a individual with unspecified qualification from United States on 2007-10-31
Patient:
Adverse reactions / side effects: Medication Error, Drug Administration Error
Suspect drug(s):
Celexa (Citalopram)
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 male receiving Celexa (Citalopram)
Reported by a individual with unspecified qualification from United States on 2007-10-22
Patient: male, weighing 71.2 kg (156.7 pounds)
Adverse reactions / side effects: Sexual Dysfunction
Suspect drug(s):
Celexa
Dosage: once a day po
Administration route: Oral
Indication: Depression
Start date: 2003-07-15
End date: 2004-12-10
Effexor XR
Dosage: once a day po
Administration route: Oral
Indication: Depression
Start date: 2005-11-22
End date: 2006-09-05
Adverse event in 32 year old female receiving Celexa (Citalopram)
Reported by a individual with unspecified qualification from United States on 2007-10-18
Patient: 32 year old female
Adverse reactions / side effects: Drug Exposure During Pregnancy, Blighted Ovum, Abortion Spontaneous, Pregnancy
Suspect drug(s):
Baclofen
Indication: Muscle Spasms
End date: 2007-03-01
Celexa
Indication: Depression
End date: 2007-03-01
Dynacin
Indication: Sweat Gland Infection
End date: 2007-03-01
Provigil
Indication: Fatigue
End date: 2007-03-01
Rebif
Dosage: 44 mcg/3 times wkly/sc
Indication: Multiple Sclerosis
Start date: 2006-03-14
End date: 2007-03-01
Relpax
Dosage: prn
Indication: Migraine
End date: 2007-03-01
Seroquel
Indication: Insomnia
End date: 2007-03-01
Vesicare
Indication: Bladder Disorder
End date: 2007-03-01
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 32 year old female receiving Celexa (Citalopram)
Reported by a consumer/non-health professional from United States on 2007-10-15
Patient: 32 year old female
Adverse reactions / side effects: Drug Exposure During Pregnancy, Abortion Spontaneous
Suspect drug(s):
Baclofen
Indication: Muscle Spasms
End date: 2007-03-01
Celexa
Indication: Depression
End date: 2007-03-01
Minocycline(minocycline Hydrochloride
Indication: Sweat Gland Infection
End date: 2007-03-01
Provigil
Indication: Fatigue
End date: 2007-03-01
Rebif
Dosage: 44 other, subcutaneous
Indication: Multiple Sclerosis
Start date: 2006-03-14
End date: 2007-03-01
Relpax
Indication: Migraine
End date: 2007-03-01
Seroquel
Indication: Insomnia
End date: 2007-03-01
Vesicare
Indication: Urinary Tract Disorder
End date: 2007-03-01
Adverse event in 30 year old female receiving Celexa (Citalopram)
Reported by a pharmacist from United States on 2007-10-15
Patient: 30 year old female
Adverse reactions / side effects: Extrapyramidal Disorder
Suspect drug(s):
Celexa (Citalopram)
Adverse event in 48 year old male receiving Celexa (Citalopram)
Reported by a lawyer from United States on 2007-10-09
Patient: 48 year old male, weighing 90.7 kg (199.6 pounds)
Adverse reactions / side effects: Aortic Injury, Excoriation, Haemorrhage, Wound, Adverse Drug Reaction, Intentional Self-Injury, Haemothorax, Injury, Heart Injury
Adverse event resulted in: death
Suspect drug(s):
Celexa (Citalopram)
Adverse event in female receiving Celexa (Citalopram)
Reported by a consumer/non-health professional from United States on 2007-10-02
Patient: female
Adverse reactions / side effects: Abortion Spontaneous
Suspect drug(s):
Baclofen
Indication: Muscle Spasms
Celexa
Indication: Depression
Minocycline HCL
Indication: Sweat Gland Infection
Provigil
Indication: Fatigue
Rebif
Indication: Multiple Sclerosis
Start date: 2006-03-14
End date: 2007-03-01
Relpax
Indication: Migraine
Seroquel
Indication: Insomnia
Vesicare
Indication: Bladder Disorder
Adverse event in female receiving Celexa (Citalopram)
Reported by a health professional (non-physician/pharmacist) from United States on 2007-10-01
Patient: female, weighing 71.8 kg (158.0 pounds)
Adverse reactions / side effects: Stomach Discomfort, Suicidal Ideation, Anxiety, Emotional Distress, Irritability, Depression, Gastrooesophageal Reflux Disease, Crying
Suspect drug(s):
Celexa
Indication: Depression
Chantix
Dosage: text:every day
Indication: Smoking Cessation Therapy
Start date: 2007-01-01
End date: 2007-01-01
Lexapro
Indication: Depression
Adverse event in female receiving Celexa (Citalopram)
Reported by a individual with unspecified qualification from Denmark on 2007-10-01
Patient: female
Adverse reactions / side effects: Apgar Score LOW, Drug Exposure During Pregnancy, Somnolence Neonatal, Meconium Increased
Suspect drug(s):
Ativan
Celexa
Zyprexa
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 3 year old female receiving Celexa (Citalopram)
Reported by a health professional (non-physician/pharmacist) from United States on 2007-07-03
Patient: 3 year old female, weighing 14.0 kg (30.8 pounds)
Adverse reactions / side effects: Breech Delivery, Macrocephaly, Autism, Drug Exposure During Pregnancy
Suspect drug(s):
Celexa (Citalopram)
Adverse event in 62 year old female receiving Celexa (Citalopram)
Reported by a consumer/non-health professional from United States on 2007-07-03
Patient: 62 year old female
Adverse reactions / side effects: Anxiety, Arthralgia, Diarrhoea, Breast Cancer Female, Joint Stiffness
Suspect drug(s):
Celebrex
Indication: Arthralgia
Start date: 2007-05-01
End date: 2007-05-01
Celebrex
Indication: Musculoskeletal Stiffness
Start date: 2007-05-01
End date: 2007-05-01
Celexa
Dosage: 10 mg qd po
Administration route: Oral
Indication: Anxiety
Start date: 2007-06-25
Celexa
Dosage: 30 mg qd po
Administration route: Oral
Indication: Anxiety
Start date: 2006-11-01
End date: 2007-01-01
Celexa
Dosage: 25 mg qd po
Administration route: Oral
Indication: Anxiety
Start date: 2005-07-01
End date: 2006-11-01
Celexa
Dosage: 20 mg qd po
Administration route: Oral
Indication: Anxiety
Start date: 2007-01-01
End date: 2007-06-24
Adverse event in 30 year old female receiving Celexa (Citalopram)
Reported by a health professional (non-physician/pharmacist) from United States on 2007-07-03
Patient: 30 year old female
Adverse reactions / side effects: Progesterone Decreased, Vomiting, Nausea, Drug Exposure During Pregnancy, Drug Exposure Before Pregnancy, Metrorrhagia
Suspect drug(s):
Celexa (Citalopram)
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
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