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Zoloft (Sertraline) - Adverse Event Reports - Life Threatening Events

 



Index of reports > Cases resulting in life threatening events (22)

     Suicide Attempt (7)Completed Suicide (5)Irritability (3)Depression (3)DRY Skin (2)Treatment Noncompliance (2)Haemodialysis (2)Suicidal Ideation (2)Abdominal Rigidity (2)Fatigue (2)

Below is the selection of adverse event reports related to Zoloft (Sertraline) that includes cases resulting in life threatening events.

Adverse event in male receiving Zoloft (Sertraline)

Reported by a physician from Denmark on 2007-10-09

Patient: male, weighing 80.0 kg (176.0 pounds)

Adverse reactions / side effects: Pancreatic Abscess

Adverse event resulted in: life threatening event, hospitalization, disablity

Suspect drug(s):
Zoloft (Sertraline)

Other drugs received by patient: Antihypertensives; Amlodipin ^orifarm^; Crestor; Simvastatin



Adverse event in male receiving Zoloft (Sertraline)

Reported by a physician from Japan on 2007-10-06

Patient: male

Adverse reactions / side effects: Panic Disorder, Somnolence, Suicidal Ideation

Adverse event resulted in: life threatening event

Suspect drug(s):
Zoloft
    Administration route: Oral
    Indication: Panic Disorder
    Start date: 2007-01-09
    End date: 2007-08-19

Dogmatyl
    Administration route: Oral
    Indication: Panic Disorder



Adverse event in female receiving Zoloft (Sertraline)

Reported by a physician from Japan on 2007-07-27

Patient: female, weighing 38.0 kg (83.6 pounds)

Adverse reactions / side effects: Oral Intake Reduced, Blood Creatine Phosphokinase Increased, Depressive Symptom, Hepatic Function Abnormal, Delusion of Reference, Pyrexia, Serotonin Syndrome, Muscle Tightness, Delusion, Hypokinesia, Thinking Abnormal, Neuroleptic Malignant Syndrome, Persecutory Delusion, Compulsions, Tremor, Anxiety, Irritability, Activities of Daily Living Impaired, Lack of Spontaneous Speech, Insomnia, Altered State of Consciousness

Adverse event resulted in: life threatening event, hospitalization

Suspect drug(s):
Zoloft
    Administration route: Oral
    Indication: Depression
    Start date: 2007-05-29
    End date: 2007-07-05

Zyprexa
    Administration route: Oral
    Indication: Delusion
    Start date: 2007-07-02
    End date: 2007-07-02

Other drugs received by patient: Reslin; Pantosin; Magvit



Adverse event in female receiving Zoloft (Sertraline)

Reported by a individual with unspecified qualification from United States on 2007-07-27

Patient: female, weighing 3.2 kg (7.0 pounds)

Adverse reactions / side effects: Fine Motor Delay, Speech Disorder Developmental, Personality Disorder, Transposition of THE Great Vessels, Fatigue, Ventricular Hypoplasia, Drug Exposure During Pregnancy, Pregnancy

Adverse event resulted in: life threatening event, hospitalization, disablity

Suspect drug(s):
Zoloft (Sertraline)



Adverse event in 46 year old female receiving Zoloft (Sertraline)

Reported by a health professional (non-physician/pharmacist) from United States on 2007-07-16

Patient: 46 year old female, weighing 74.4 kg (163.7 pounds)

Adverse reactions / side effects: Abdominal Pain, Somnolence, Treatment Noncompliance, Laboratory Test Abnormal, Fatigue, Chest Pain, Dizziness, Temperature Intolerance, Injury, Depression, Cough, Viral Load Increased, Chromaturia, DRY Skin, Poisoning Deliberate, Haemodialysis, Irritability, Renal Failure, Abdominal Rigidity, Weight, Suicide Attempt, Bronchitis, Asthenia

Adverse event resulted in: life threatening event, hospitalization, disablity

Suspect drug(s):
PEG-Intron
    Dosage: 96 mcg; qw; sc
    Indication: Hepatitis C
    Start date: 2001-11-23
    End date: 2002-02-08

Rebetol
    Dosage: 1000 mg; qd; po
    Administration route: Oral
    Indication: Hepatitis C
    Start date: 2001-11-23
    End date: 2002-02-15

Zoloft
    Dosage: 100 mg; qd; po
    Administration route: Oral
    Indication: Depression

Antifreeze (Ethylene Glycol)
    Dosage: once; po
    Administration route: Oral
    Indication: Suicide Attempt
    Start date: 2002-02-16
    End date: 2002-02-16

Other drugs received by patient: Atenolol; Nexium; Premarin; Prilosec; Norvasc



Adverse event in 62 year old female receiving Zoloft (Sertraline)

Reported by a physician from Germany on 2007-06-29

Patient: 62 year old female

Adverse reactions / side effects: Agitation, Restlessness, Intentional Overdose, Suicide Attempt, Suicidal Ideation

Adverse event resulted in: life threatening event, hospitalization

Suspect drug(s):
Zoloft (Sertraline)

Other drugs received by patient: Mirtazapine



Adverse event in 37 year old female receiving Zoloft (Sertraline)

Reported by a consumer/non-health professional from United States on 2007-06-12

Patient: 37 year old female, weighing 81.6 kg (179.6 pounds)

Adverse reactions / side effects: Pelvic Fracture, Psychotic Disorder, Pain, Abnormal Behaviour, Arthritis

Adverse event resulted in: life threatening event, hospitalization

Suspect drug(s):
Zoloft
    Dosage: daily
    Indication: Narcolepsy
    Start date: 1998-04-01
    End date: 1998-07-13

Ionamin
    Dosage: daily
    Start date: 1998-04-01
    End date: 1998-07-13



Adverse event in 41 year old female receiving Zoloft (Sertraline)

Reported by a consumer/non-health professional from United States on 2007-06-04

Patient: 41 year old female, weighing 81.6 kg (179.6 pounds)

Adverse reactions / side effects: Mental Impairment, Suicide Attempt

Adverse event resulted in: life threatening event

Suspect drug(s):
Zoloft (Sertraline)

Other drugs received by patient: Wellbutrin



Adverse event in 14 year old female receiving Zoloft (Sertraline)

Reported by a consumer/non-health professional from United States on 2007-05-17

Patient: 14 year old female, weighing 72.6 kg (159.7 pounds)

Adverse reactions / side effects: Nightmare, Fear, Feeling Abnormal, Crying

Adverse event resulted in: life threatening event

Suspect drug(s):
Zoloft (Sertraline)



Adverse event in 27 year old female receiving Zoloft (Sertraline)

Reported by a individual with unspecified qualification from United States on 2007-04-19

Patient: 27 year old female, weighing 84.4 kg (185.6 pounds)

Adverse reactions / side effects: Therapeutic Response Unexpected With Drug Substitution, Depression, Feeling Abnormal, Hypersomnia

Adverse event resulted in: life threatening event

Suspect drug(s):
Zoloft
    Dosage: 200mg 2 100mg tab/day po
    Administration route: Oral
    Indication: Anxiety
    Start date: 2007-01-23
    End date: 2007-03-06

Zoloft
    Dosage: 200mg 2 100mg tab/day po
    Administration route: Oral
    Indication: Depression
    Start date: 2007-01-23
    End date: 2007-03-06



Adverse event in 32 year old female receiving Zoloft (Sertraline)

Reported by a health professional (non-physician/pharmacist) from United States on 2007-04-16

Patient: 32 year old female, weighing 90.7 kg (199.6 pounds)

Adverse reactions / side effects: Pain, Suicide Attempt

Adverse event resulted in: life threatening event, hospitalization, disablity

Suspect drug(s):
Oxycontin
    Dosage: 60 ml
    Indication: Surgery
    Start date: 2006-06-12
    End date: 2007-04-04

Zoloft



Adverse event in male receiving Zoloft (Sertraline)

Reported by a physician from Japan on 2007-04-11

Patient: male

Adverse reactions / side effects: Feeling of Despair, Injury Asphyxiation, Anxiety, Insomnia, Completed Suicide, Psychiatric Symptom, Central Nervous System Stimulation, Depressed Mood

Adverse event resulted in: death, life threatening event

Suspect drug(s):
Zoloft (Sertraline)

Other drugs received by patient: Norvasc; Solanax; Gasmotin; Myslee; Tenormin; Nitorol R; Diltiazem HCL; Magnesium Oxide; Pursennid; Amoxan



Adverse event in 63 year old male receiving Zoloft (Sertraline)

Reported by a pharmacist from United States on 2007-03-28

Patient: 63 year old male, weighing 77.1 kg (169.6 pounds)

Adverse reactions / side effects: Torsade DE Pointes, Cardio-Respiratory Arrest, Atrial Fibrillation, Treatment Noncompliance

Adverse event resulted in: life threatening event

Suspect drug(s):
Methadone HCL
    Dosage: 80mg qam po
    Administration route: Oral
    Indication: Drug Dependence

Zoloft
    Dosage: 150mg qam po
    Administration route: Oral



Adverse event in 33 year old male receiving Zoloft (Sertraline)

Reported by a individual with unspecified qualification from United States on 2007-03-26

Patient: 33 year old male, weighing 97.5 kg (214.6 pounds)

Adverse reactions / side effects: Agitation, Condition Aggravated, Loss of Consciousness, Delusion, Alcoholism, Psychiatric Symptom, Suicide Attempt, Anger, Depression, Emotional Disorder, Drug Dependence

Adverse event resulted in: life threatening event

Suspect drug(s):
Zoloft (Sertraline)



Adverse event in 65 year old female receiving Zoloft (Sertraline)

Reported by a individual with unspecified qualification from United States on 2007-03-26

Patient: 65 year old female, weighing 54.9 kg (120.7 pounds)

Adverse reactions / side effects: Flushing, Blood Pressure Increased, Feeling Hot, Heart Rate Increased, Thyroid Disorder, Erythema

Adverse event resulted in: life threatening event, hospitalization

Suspect drug(s):
Zoloft (Sertraline)



Adverse event in 63 year old female receiving Zoloft (Sertraline)

Reported by a physician from Japan on 2007-03-07

Patient: 63 year old female

Adverse reactions / side effects: Completed Suicide

Adverse event resulted in: death, life threatening event

Suspect drug(s):
Zoloft (Sertraline)



Adverse event in 16 year old female receiving Zoloft (Sertraline)

Reported by a physician from Japan on 2007-03-07

Patient: 16 year old female

Adverse reactions / side effects: Completed Suicide

Adverse event resulted in: death, life threatening event

Suspect drug(s):
Zoloft (Sertraline)



Adverse event in female receiving Zoloft (Sertraline)

Reported by a pharmacist from United States on 2007-03-02

Patient: female, weighing 56.0 kg (123.2 pounds)

Adverse reactions / side effects: Vomiting, Incorrect Dose Administered, Suicide Attempt, Intentional Self-Injury, Loss of Consciousness

Adverse event resulted in: life threatening event, hospitalization

Suspect drug(s):
Zoloft
    Dosage: 1250 mg once po
    Administration route: Oral
    Indication: Depression
    Start date: 2007-02-23
    End date: 2007-02-26

Seroquel
    Dosage: 2000 mg once po
    Administration route: Oral
    Indication: Insomnia
    Start date: 2007-02-23
    End date: 2007-02-26



Adverse event in 46 year old female receiving Zoloft (Sertraline)

Reported by a health professional (non-physician/pharmacist) from United States on 2007-02-07

Patient: 46 year old female, weighing 74.4 kg (163.7 pounds)

Adverse reactions / side effects: Abdominal Pain, Hepatitis C, Chest Pain, Dizziness, Injury, Alanine Aminotransferase Abnormal, Cough, Blood Test Abnormal, Chromaturia, DRY Skin, Exposure TO Toxic Agent, Haemodialysis, Irritability, Blood Glucose Decreased, Renal Failure, Abdominal Rigidity, Suicide Attempt, Bronchitis, Aspartate Aminotransferase Abnormal

Adverse event resulted in: life threatening event, hospitalization, disablity

Suspect drug(s):
PEG-Intron
    Dosage: 96 mcg;qw;sc
    Indication: Hepatitis C
    Start date: 2001-11-23
    End date: 2002-02-08

Rebetol
    Dosage: see image
    Administration route: Oral
    Indication: Hepatitis C
    Start date: 2001-11-23
    End date: 2002-02-15

Zoloft
    Dosage: 100 mg;qd;po
    Administration route: Oral
    Indication: Depression

Other drugs received by patient: Atenolol; Nexium; Premarin; Prilosec; Norvasc



Adverse event in 15 year old female receiving Zoloft (Sertraline)

Reported by a physician from Japan on 2007-01-19

Patient: 15 year old female

Adverse reactions / side effects: Completed Suicide

Adverse event resulted in: death, life threatening event

Suspect drug(s):
Zoloft (Sertraline)



Adverse event in 63 year old female receiving Zoloft (Sertraline)

Reported by a physician from Japan on 2007-01-19

Patient: 63 year old female

Adverse reactions / side effects: Completed Suicide

Adverse event resulted in: death, life threatening event

Suspect drug(s):
Zoloft (Sertraline)



Adverse event in female receiving Zoloft (Sertraline)

Reported by a physician from Australia on 2007-01-16

Patient: female, weighing 70.0 kg (154.0 pounds)

Adverse reactions / side effects: Physical Assault, Delusional Disorder, Persecutory Type

Adverse event resulted in: life threatening event, hospitalization

Suspect drug(s):
Buscopan
    Indication: Abdominal Pain
    Start date: 2005-12-28
    End date: 2005-12-29

DI-Gesic
    Administration route: Oral
    End date: 2005-12-29

Lomotil
    Administration route: Oral
    Indication: Diarrhoea
    Start date: 2005-12-28
    End date: 2005-12-29

Diazepam
    Indication: Anxiety Disorder

Zoloft
    Administration route: Oral
    Indication: Depression

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