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Index of reports
> Cases resulting in hospitalization (139)
Below is the selection of adverse event reports related to Lexapro (Escitalopram) that includes cases resulting in hospitalization.
Reports 1 - 25 of 139 Next >>
Adverse event in 55 year old female receiving Lexapro (Escitalopram)
Reported by a health professional (non-physician/pharmacist) from United States on 2007-10-25
Patient: 55 year old female
Adverse reactions / side effects: Tinnitus, Dyspnoea, Drug Interaction, Serotonin Syndrome, Swollen Tongue, Intervertebral Disc Degeneration, Dizziness, Sinusitis, Feeling Abnormal
Adverse event resulted in: hospitalization
Suspect drug(s):
Lexapro
Dosage: 10 mg qd po
Administration route: Oral
Indication: Anxiety
Start date: 2006-12-01
End date: 2007-10-09
Lexapro
Dosage: 10 mg qd po
Administration route: Oral
Indication: Depression
Start date: 2006-12-01
End date: 2007-10-09
Delsym
Indication: Cough
Start date: 2007-09-06
End date: 2007-09-29
Other drugs received by patient: Levothyroxine Sodium; Atacand; Hydrochlorothiazide; Vytorin
Adverse event in 49 year old male receiving Lexapro (Escitalopram)
Reported by a physician from United States on 2007-10-25
Patient: 49 year old male
Adverse reactions / side effects: Alcoholism
Adverse event resulted in: hospitalization
Suspect drug(s):
Lexapro
Dosage: 20 mg qd po
Administration route: Oral
Indication: Major Depression
Start date: 2007-06-04
End date: 2007-08-06
Lexapro
Dosage: 10 mg qd po
Administration route: Oral
Indication: Major Depression
Start date: 2006-08-07
End date: 2007-06-03
Other drugs received by patient: Tylenol PM (Acetaminophen); Celebrex
Adverse event in receiving Lexapro (Escitalopram)
Reported by a health professional (non-physician/pharmacist) from United States on 2007-10-23
Patient:
Adverse reactions / side effects: Haemoglobin Decreased, Atelectasis, Haematocrit Decreased, Dyspnoea, Pneumonia, Chest Pain, Myocardial Infarction, Blood Glucose Increased
Adverse event resulted in: life threatening event, hospitalization
Suspect drug(s):
Methadone HCL
Dosage: 10 mg, 1-2 tablet, q6hr
Administration route: Oral
Indication: Pain
Methadone HCL
Dosage: 40 mg, bid
Administration route: Oral
Start date: 2007-08-20
CP-751,871
Dosage: 1560 mg, single (1 dose q 21 days)
Indication: non-Small Cell Lung Cancer
Start date: 2007-06-20
End date: 2007-06-20
CP-751,871
Dosage: 1600 mg, single (1 dose q 21 days)
Start date: 2007-07-11
End date: 2007-07-11
CP-751,871
Dosage: 1540 mg, single (1 dose q 21 days)
Start date: 2007-08-01
Taxol
Dosage: 395 mg, single (1 dose q 21 days)
Indication: non-Small Cell Lung Cancer
Start date: 2007-06-19
End date: 2007-06-19
Taxol
Dosage: 382 mg, single (1 dose q 21 days)
Start date: 2007-07-10
End date: 2007-07-10
Taxol
Dosage: 329 mg, single (1 dose q 21 days)
Start date: 2007-07-31
End date: 2007-07-31
Carboplatin
Dosage: 620 mg, single (1 dose q 21 days)
Indication: non-Small Cell Lung Cancer
Start date: 2007-06-19
End date: 2007-06-19
Carboplatin
Dosage: 564 mg, single ( 1 dose q 21 days)
Start date: 2007-07-10
End date: 2007-07-10
Carboplatin
Dosage: 516 mg, single (1 dose q 21 days)
Start date: 2007-07-31
Lexapro
Dosage: 10 mg, qd
Administration route: Oral
Start date: 2007-06-12
Coumadin
Dosage: 5 mg, qd
Administration route: Oral
Start date: 2007-07-31
Lovenox
Dosage: 10 mg, q6-8hr
Administration route: Oral
Start date: 2007-06-12
Other drugs received by patient: Reglan / 00041901 /; Nitroglycerin; Gabapentin; Oxycodone HCL
Adverse event in 79 year old male receiving Lexapro (Escitalopram)
Reported by a consumer/non-health professional from United States on 2007-10-23
Patient: 79 year old male
Adverse reactions / side effects: Nausea, Diarrhoea, Dehydration
Adverse event resulted in: hospitalization
Suspect drug(s):
Lexapro (Escitalopram)
Other drugs received by patient: Plavix; Imdur; Lopressor; Protonix
Adverse event in 72 year old male receiving Lexapro (Escitalopram)
Reported by a health professional (non-physician/pharmacist) from United States on 2007-10-18
Patient: 72 year old male, weighing 76.9 kg (169.2 pounds)
Adverse reactions / side effects: Dyspnoea, Chest Pain
Adverse event resulted in: life threatening event, hospitalization
Suspect drug(s):
Lovenox
Indication: Anticoagulant Therapy
Start date: 2007-07-27
Methadone HCL
Administration route: Oral
Indication: Drug USE FOR Unknown Indication
Start date: 2007-01-01
Lexapro
Administration route: Oral
Indication: Drug USE FOR Unknown Indication
Start date: 2007-06-12
Coumadin
Administration route: Oral
Indication: Anticoagulant Therapy
Start date: 2007-07-31
Other drugs received by patient: Reglan / 00041901 /; Nitroglycerin; Gabapentin; CP-751, 871 (Investigational Drug); CP-751, 871 (Investigational Drug); CP-751, 871 (Investigational Drug); Paclitaxel; Paclitaxel; Paclitaxel; Carboplatin; Carboplatin; Carboplatin
Adverse event in 47 year old male receiving Lexapro (Escitalopram)
Reported by a consumer/non-health professional from United States on 2007-10-17
Patient: 47 year old male, weighing 90.7 kg (199.6 pounds)
Adverse reactions / side effects: Weight Increased, Grand MAL Convulsion, Overdose, Haemorrhagic Stroke, Blood Cholesterol Increased
Adverse event resulted in: hospitalization
Suspect drug(s):
Lexapro (Escitalopram)
Other drugs received by patient: Unknown Hypertension Medication (Nos)
Adverse event in 57 year old male receiving Lexapro (Escitalopram)
Reported by a physician from United States on 2007-10-15
Patient: 57 year old male, weighing 79.8 kg (175.6 pounds)
Adverse reactions / side effects: Cardiac Murmur, Tremor, Aggression, Suicidal Ideation, Mania, Dehydration, Depression, Decreased Appetite
Adverse event resulted in: hospitalization
Suspect drug(s):
Lexapro
Dosage: 10 mg qd po
Administration route: Oral
Indication: Depression
Start date: 2007-02-05
End date: 2007-03-16
Wellbutrin XL
Dosage: 300 mg qd
Indication: Depression
Start date: 2007-02-12
End date: 2007-03-16
Alcohol
Start date: 2007-03-17
Other drugs received by patient: Lotrel
Adverse event in female receiving Lexapro (Escitalopram)
Reported by a physician from United States on 2007-10-15
Patient: female
Adverse reactions / side effects: Hyponatraemia
Adverse event resulted in: hospitalization
Suspect drug(s):
Lexapro (Escitalopram)
Other drugs received by patient: Numerous Medications (Nos)
Adverse event in 60 year old male receiving Lexapro (Escitalopram)
Reported by a physician from United States on 2007-10-15
Patient: 60 year old male
Adverse reactions / side effects: Burning Sensation, Flushing, Nausea, Headache, Asthenia
Adverse event resulted in: hospitalization
Suspect drug(s):
Lexapro
Dosage: 10 mg qd po
Administration route: Oral
Indication: Anxiety
Start date: 2007-05-09
End date: 2007-05-11
Lexapro
Dosage: 10 mg qd po
Administration route: Oral
Indication: Depression
Start date: 2007-05-09
End date: 2007-05-11
Other drugs received by patient: Cardizem; Lisinopril; Tricor; Metformin HCL; Glucotrol; Cialis; Lortabs (Acetaminophen / Hydrocodone); Nexium; Aspirin
Adverse event in 17 year old male receiving Lexapro (Escitalopram)
Reported by a physician from United States on 2007-10-15
Patient: 17 year old male
Adverse reactions / side effects: Anxiety, Thinking Abnormal, Nausea, Hypoaesthesia Facial, Insomnia, Depression, Hypoaesthesia, Suicidal Ideation
Adverse event resulted in: hospitalization
Suspect drug(s):
Lexapro
Dosage: 20 mg qd po
Administration route: Oral
Indication: Depression
Start date: 2006-01-01
End date: 2007-05-31
Risperdal
Dosage: 20 mg qd po
Administration route: Oral
Indication: Depression
Start date: 2007-05-31
End date: 2007-06-01
Other drugs received by patient: Ativan; Lamictal
Adverse event in 53 year old female receiving Lexapro (Escitalopram)
Reported by a physician from United States on 2007-10-15
Patient: 53 year old female
Adverse reactions / side effects: Anxiety, Hypersensitivity, Nausea, Headache, Decreased Appetite, Lethargy
Adverse event resulted in: hospitalization
Suspect drug(s):
Lexapro
Dosage: 10 mg qd po
Administration route: Oral
Indication: Anxiety
Start date: 2005-05-25
End date: 2005-05-25
Lexapro
Dosage: 10 mg qd po
Administration route: Oral
Indication: Depression
Start date: 2005-05-25
End date: 2005-05-25
Other drugs received by patient: Lantus; Glipizide; Diovan
Adverse event in 53 year old female receiving Lexapro (Escitalopram)
Reported by a health professional (non-physician/pharmacist) from United States on 2007-10-15
Patient: 53 year old female, weighing 84.4 kg (185.6 pounds)
Adverse reactions / side effects: Gastrointestinal Haemorrhage
Adverse event resulted in: hospitalization
Suspect drug(s):
Lexapro (Escitalopram)
Other drugs received by patient: Zanaflex; Norvasc; Hydrochlorothiazide
Adverse event in 73 year old female receiving Lexapro (Escitalopram)
Reported by a physician from United States on 2007-10-15
Patient: 73 year old female
Adverse reactions / side effects: Depression
Adverse event resulted in: hospitalization
Suspect drug(s):
Lexapro (Escitalopram)
Adverse event in male receiving Lexapro (Escitalopram)
Reported by a physician from United States on 2007-10-15
Patient: male
Adverse reactions / side effects: Hyponatraemia
Adverse event resulted in: hospitalization
Suspect drug(s):
Lexapro
Dosage: 10 mg qd po
Administration route: Oral
Start date: 2007-01-01
End date: 2007-01-01
Hydrochlorothiazide
Indication: Hypertension
Adverse event in receiving Lexapro (Escitalopram)
Reported by a physician from United States on 2007-10-15
Patient:
Adverse reactions / side effects: Overdose
Adverse event resulted in: hospitalization
Suspect drug(s):
Lexapro
Start date: 2007-04-01
Lexapro
Adverse event in 24 year old female receiving Lexapro (Escitalopram)
Reported by a physician from United States on 2007-10-15
Patient: 24 year old female
Adverse reactions / side effects: Syncope, Tension Headache, Feeling Jittery, Heart Rate Increased, Hypoaesthesia
Adverse event resulted in: hospitalization
Suspect drug(s):
Lexapro
Dosage: 10 mg qd po
Administration route: Oral
Indication: Anxiety
Start date: 2007-07-21
End date: 2007-07-22
Lexapro
Dosage: 10 mg qd po
Administration route: Oral
Indication: Panic Reaction
Start date: 2007-07-21
End date: 2007-07-22
Other drugs received by patient: Xanax
Adverse event in 44 year old female receiving Lexapro (Escitalopram)
Reported by a physician from United States on 2007-10-15
Patient: 44 year old female
Adverse reactions / side effects: Syncope
Adverse event resulted in: hospitalization
Suspect drug(s):
Lexapro (Escitalopram)
Adverse event in 38 year old female receiving Lexapro (Escitalopram)
Reported by a consumer/non-health professional from United States on 2007-10-15
Patient: 38 year old female
Adverse reactions / side effects: Hypersensitivity, Drug Ineffective
Adverse event resulted in: hospitalization
Suspect drug(s):
Lexapro
Dosage: 10 mg qd po
Administration route: Oral
Indication: Major Depression
Start date: 2005-01-01
End date: 2005-01-01
Lexapro
Dosage: 20 mg qd po
Administration route: Oral
Indication: Major Depression
Start date: 2007-04-14
End date: 2007-05-31
Other drugs received by patient: Prozac; Effexor
Adverse event in 84 year old female receiving Lexapro (Escitalopram)
Reported by a health professional (non-physician/pharmacist) from United States on 2007-10-15
Patient: 84 year old female
Adverse reactions / side effects: Blood Sodium Decreased
Adverse event resulted in: hospitalization
Suspect drug(s):
Lexapro
Dosage: 10 mg qd po
Administration route: Oral
Indication: Depression
Start date: 2007-04-23
End date: 2007-04-01
Avalide
Indication: Hypertension
End date: 2007-04-01
Other drugs received by patient: Atenolol
Adverse event in 32 year old male receiving Lexapro (Escitalopram)
Reported by a physician from United States on 2007-10-15
Patient: 32 year old male
Adverse reactions / side effects: Pulmonary Embolism
Adverse event resulted in: hospitalization
Suspect drug(s):
Lexapro (Escitalopram)
Other drugs received by patient: Diamox
Adverse event in 79 year old female receiving Lexapro (Escitalopram)
Reported by a physician from United States on 2007-10-15
Patient: 79 year old female
Adverse reactions / side effects: Hyponatraemia
Adverse event resulted in: hospitalization
Suspect drug(s):
Lexapro (Escitalopram)
Adverse event in 19 year old male receiving Lexapro (Escitalopram)
Reported by a consumer/non-health professional from United States on 2007-10-15
Patient: 19 year old male
Adverse reactions / side effects: Fatigue, Pancreatitis
Adverse event resulted in: hospitalization
Suspect drug(s):
Lexapro
Dosage: 10 mg qd po
Administration route: Oral
Indication: Depression
Start date: 2007-01-01
Alcohol
Other drugs received by patient: Allergy Medication (Nos)
Adverse event in 41 year old male receiving Lexapro (Escitalopram)
Reported by a physician from United States on 2007-10-15
Patient: 41 year old male
Adverse reactions / side effects: Agitation, Speech Disorder, Intentional Overdose, Depression, Suicidal Ideation, Tremor
Adverse event resulted in: hospitalization
Suspect drug(s):
Lexapro
Dosage: 20 mg qd po
Administration route: Oral
Indication: Depression
Start date: 2004-07-01
Lexapro
Dosage: 20 mg qd po
Administration route: Oral
Indication: Depression
End date: 2006-05-01
Lexapro
Dosage: 20 mg qd po
Administration route: Oral
Indication: Depression
Start date: 2006-05-01
End date: 2006-07-01
Lexapro
Indication: Depression
Start date: 2006-05-01
End date: 2006-05-01
Adverse event in female receiving Lexapro (Escitalopram)
Reported by a health professional (non-physician/pharmacist) from United States on 2007-10-15
Patient: female
Adverse reactions / side effects: Blood Sodium Decreased
Adverse event resulted in: hospitalization
Suspect drug(s):
Lexapro (Escitalopram)
Adverse event in 18 year old female receiving Lexapro (Escitalopram)
Reported by a health professional (non-physician/pharmacist) from United States on 2007-10-09
Patient: 18 year old female
Adverse reactions / side effects: Dysphoria, Alcohol USE, Psychotic Disorder, Drug Withdrawal Syndrome, Treatment Noncompliance
Adverse event resulted in: hospitalization
Suspect drug(s):
Lexapro
Indication: Anxiety
Start date: 2007-07-10
Lexapro
Indication: Depression
Start date: 2007-07-10
Alcohol
Start date: 2007-09-21
End date: 2007-09-21
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