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Index of reports
> All cases (434)
Below is the selection of adverse event reports related to Lexapro (Escitalopram) that includes all cases.
Reports 1 - 25 of 434 Next >>
Adverse event in 68 year old female receiving Lexapro (Escitalopram)
Reported by a physician from United States on 2007-10-30
Patient: 68 year old female
Adverse reactions / side effects: Drug Level Above Therapeutic, Arrhythmia
Adverse event resulted in: death
Suspect drug(s):
Lexapro (Escitalopram)
Other drugs received by patient: Fentanyl; Hydrocodone Bitartrate
Adverse event in 83 year old female receiving Lexapro (Escitalopram)
Reported by a physician from United States on 2007-10-26
Patient: 83 year old female
Adverse reactions / side effects: Drug Ineffective
Suspect drug(s):
Lexapro
Indication: Drug USE FOR Unknown Indication
End date: 2007-08-18
Vaprisol
Dosage: iv drip
Indication: Hyponatraemia
Start date: 2007-08-16
End date: 2007-08-21
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 physician from United States on 2007-10-25
Patient:
Adverse reactions / side effects: Road Traffic Accident, Multiple Drug Overdose
Suspect drug(s):
Effexor
Lexapro
Adverse event in receiving Lexapro (Escitalopram)
Reported by a physician from United States on 2007-10-25
Patient:
Adverse reactions / side effects: Transaminases Increased
Suspect drug(s):
Lexapro
Dosage: 10 mg qd po
Administration route: Oral
Lexapro
Dosage: 10 mg qd po
Administration route: Oral
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):
Delsym
Indication: Cough
Start date: 2007-09-06
End date: 2007-09-29
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
Other drugs received by patient: Levothyroxine Sodium; Atacand; Hydrochlorothiazide; Vytorin
Adverse event in male receiving Lexapro (Escitalopram)
Reported by a physician from United States on 2007-10-24
Patient: male, weighing 66.2 kg (145.7 pounds)
Adverse reactions / side effects: NO Therapeutic Response, Condition Aggravated, Headache
Suspect drug(s):
Lexapro (Escitalopram)
Other drugs received by patient: Relpax; Phenergan HCL; Excedrin (Migraine); Calcium; Magnesium Sulfate; Amoxicillin; Nasarel; Hydrocodone; Ibuprofen; Vicodin; Naprosyn; Aspirin; Midrin; Fish OIL; Trazodone HCL; Zoloft
Adverse event in 46 year old female receiving Lexapro (Escitalopram)
Reported by a physician from United States on 2007-10-24
Patient: 46 year old female, weighing 64.0 kg (140.8 pounds)
Adverse reactions / side effects: Vomiting, Dyspnoea, Diarrhoea, Dizziness, Asthenia, Loss of Consciousness
Suspect drug(s):
Aleve
Dosage: total daily dose: 220 mg unit dose: 220 mg
Administration route: Oral
Indication: Back Pain
Start date: 2007-06-05
End date: 2007-06-05
Lexapro
Dosage: total daily dose: 10 mg unit dose: 10 mg
Administration route: Oral
Indication: Drug USE FOR Unknown Indication
Rebif
Dosage: unit dose: 44 ?g
Indication: Multiple Sclerosis
Start date: 2006-07-17
Other drugs received by patient: Femhrt
Adverse event in 76 year old male receiving Lexapro (Escitalopram)
Reported by a consumer/non-health professional from United States on 2007-10-23
Patient: 76 year old male, weighing 81.6 kg (179.6 pounds)
Adverse reactions / side effects: Completed Suicide
Adverse event resulted in: death
Suspect drug(s):
Lexapro (Escitalopram)
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 55 year old female receiving Lexapro (Escitalopram)
Reported by a physician from United States on 2007-10-23
Patient: 55 year old female, weighing 81.6 kg (179.6 pounds)
Adverse reactions / side effects: Drug Interaction, Convulsion
Suspect drug(s):
Lexapro
Dosage: 10 mg qd oral
Administration route: Oral
Indication: Depression
Provigil
Dosage: 100 mg bid oral
Administration route: Oral
Indication: Hypersomnia
Start date: 2007-09-07
End date: 2007-09-08
Provigil
Dosage: 100 mg qd oral
Administration route: Oral
Indication: Hypersomnia
Start date: 2007-09-09
Other drugs received by patient: Lorazepam; Zyrtec; Hormone Replacement Therapy (Unspecified)
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):
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
Coumadin
Dosage: 5 mg, qd
Administration route: Oral
Start date: 2007-07-31
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
Lexapro
Dosage: 10 mg, qd
Administration route: Oral
Start date: 2007-06-12
Lovenox
Dosage: 10 mg, q6-8hr
Administration route: Oral
Start date: 2007-06-12
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
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
Other drugs received by patient: Reglan / 00041901 /; Nitroglycerin; Gabapentin; Oxycodone HCL
Adverse event in 17 year old male receiving Lexapro (Escitalopram)
Reported by a physician from United States on 2007-10-18
Patient: 17 year old male
Adverse reactions / side effects: Suicidal Behaviour, Dissociation, Wound, Dissociative Amnesia, Joint Injury
Suspect drug(s):
Lexapro
Dosage: 20 mg qd po
Administration route: Oral
Indication: Anxiety
Start date: 2007-09-11
Lexapro
Dosage: 20 mg qd po
Administration route: Oral
Indication: Depression
Start date: 2007-09-11
Other drugs received by patient: Lamictal; Depakote
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):
Coumadin
Administration route: Oral
Indication: Anticoagulant Therapy
Start date: 2007-07-31
Lexapro
Administration route: Oral
Indication: Drug USE FOR Unknown Indication
Start date: 2007-06-12
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
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 45 year old female receiving Lexapro (Escitalopram)
Reported by a health professional (non-physician/pharmacist) from Ireland on 2007-10-18
Patient: 45 year old female
Adverse reactions / side effects: Vaginal Haemorrhage
Adverse event resulted in: disablity
Suspect drug(s):
Lexapro (Escitalopram)
Other drugs received by patient: Amoxicillin
Adverse event in 60 year old female receiving Lexapro (Escitalopram)
Reported by a consumer/non-health professional from United States on 2007-10-17
Patient: 60 year old female
Adverse reactions / side effects: Dysstasia, Abasia
Suspect drug(s):
Lexapro
Dosage: 20 mg qd po
Administration route: Oral
Indication: Anxiety
Start date: 2006-01-01
Lexapro
Dosage: 20 mg qd po
Administration route: Oral
Indication: Depression
Start date: 2006-01-01
Other drugs received by patient: Fosamax; Tofranil
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 65 year old male receiving Lexapro (Escitalopram)
Reported by a health professional (non-physician/pharmacist) from Ireland on 2007-10-17
Patient: 65 year old male
Adverse reactions / side effects: Intentional Overdose, Completed Suicide
Adverse event resulted in: death
Suspect drug(s):
Lexapro
Dosage: 10 mg qd po
Administration route: Oral
Indication: Depression
End date: 2007-06-18
Paraquat
Start date: 2007-08-23
End date: 2007-08-23
Other drugs received by patient: Pravastatin Sodium; Mirtazapine
Adverse event in 42 year old female receiving Lexapro (Escitalopram)
Reported by a consumer/non-health professional from United States on 2007-10-17
Patient: 42 year old female
Adverse reactions / side effects: Dysarthria, Impaired Driving Ability, Loss of Employment, Motor Dysfunction, Somnolence, Lethargy
Suspect drug(s):
Lexapro
Indication: Anxiety
Start date: 2007-02-01
End date: 2007-04-01
Lexapro
Indication: Depression
Start date: 2007-02-01
End date: 2007-04-01
Adverse event in 42 year old female receiving Lexapro (Escitalopram)
Reported by a health professional (non-physician/pharmacist) from United States on 2007-10-16
Patient: 42 year old female
Adverse reactions / side effects: Thrombosis, Hypokalaemia, Convulsion, Drug Toxicity, Cholelithiasis, Road Traffic Accident, Overdose, Peroneal Muscular Atrophy
Adverse event resulted in: death
Suspect drug(s):
Lexapro (Escitalopram)
Other drugs received by patient: Potassium Replacement
Adverse event in 58 year old male receiving Lexapro (Escitalopram)
Reported by a health professional (non-physician/pharmacist) from Denmark on 2007-10-16
Patient: 58 year old male
Adverse reactions / side effects: Agitation, Contusion, Incorrect Dose Administered, Condition Aggravated, Skull Fracture, Traumatic Brain Injury, Completed Suicide, GUN Shot Wound
Adverse event resulted in: death
Suspect drug(s):
Lexapro (Escitalopram)
Other drugs received by patient: Xanax
Adverse event in 77 year old female receiving Lexapro (Escitalopram)
Reported by a consumer/non-health professional from United States on 2007-10-15
Patient: 77 year old female
Adverse reactions / side effects: Depression, Suicidal Ideation
Suspect drug(s):
Lexapro
Dosage: 20 mg qd po
Administration route: Oral
Indication: Anxiety
Start date: 2007-04-15
Lexapro
Dosage: 20 mg qd po
Administration route: Oral
Indication: Depression
Start date: 2007-04-15
Other drugs received by patient: Xanax
Adverse event in receiving Lexapro (Escitalopram)
Reported by a health professional (non-physician/pharmacist) from United States on 2007-10-15
Patient:
Adverse reactions / side effects: Loss of Consciousness
Suspect drug(s):
Lexapro (Escitalopram)
Adverse event in receiving Lexapro (Escitalopram)
Reported by a physician from United States on 2007-10-15
Patient:
Adverse reactions / side effects: Hyponatraemia
Suspect drug(s):
Lexapro (Escitalopram)
Adverse event in female receiving Lexapro (Escitalopram)
Reported by a consumer/non-health professional from United States on 2007-10-15
Patient: female
Adverse reactions / side effects: Suicidal Ideation
Suspect drug(s):
Lexapro (Escitalopram)
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