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Index of reports
> Cases resulting in life threatening events (8)
Below is the selection of adverse event reports related to Promethazine that includes cases resulting in life threatening events.
Adverse event in female receiving Promethazine
Reported by a physician from Germany on 2007-10-31
Patient: female
Adverse reactions / side effects: Overdose, Aspiration, Hypotension, Coma, Drug Abuser, Polyuria, Suicide Attempt
Adverse event resulted in: life threatening event
Suspect drug(s):
Acetaminophen
Administration route: Oral
Buscopan
Administration route: Oral
Carbamazepine
Administration route: Oral
Cymbalta
Administration route: Oral
Diazepam
Administration route: Oral
Diclo
Administration route: Oral
Dociton
Administration route: Oral
Promethazine
Administration route: Oral
Trimipramine Maleate
Administration route: Oral
ZOP
Administration route: Oral
Adverse event in 43 year old male receiving Promethazine
Reported by a pharmacist from United States on 2007-07-30
Patient: 43 year old male, weighing 78.0 kg (171.6 pounds)
Adverse reactions / side effects: Nausea, Unresponsive TO Stimuli, Hyperhidrosis, Malaise, Dizziness, Bradycardia, Cold Sweat, Cardiac Arrest
Adverse event resulted in: life threatening event
Suspect drug(s):
Lovenox
Dosage: 40mg qd subcutaneous one dose
Indication: Cerebrovascular Accident Prophylaxis
Promethazine
Dosage: 25 mg iv x 1 one dose
Indication: Nausea
Adverse event in 44 year old female receiving Promethazine
Reported by a health professional (non-physician/pharmacist) from United States on 2007-07-25
Patient: 44 year old female
Adverse reactions / side effects: Agitation, Respiratory Rate Increased, Paranoia, Blood Pressure Systolic Increased, Nausea, Illusion, Drug Interaction, Platelet Count Increased, Wound Infection, Serotonin Syndrome, Pyrexia, Disorientation, Heart Rate Increased, Depression, White Blood Cell Count Increased
Adverse event resulted in: life threatening event
Suspect drug(s):
Citalopram Hydrobromide
Dosage: 20 mg, oral; 40 mg, oral
Administration route: Oral
Indication: Depression
Meperidine HCL
Dosage: total dose of 230 mg over 8 hours, parenteral
Indication: Depression
Promethazine
Other drugs received by patient: Hydromorphone HCL; Hydrocodone Bitartrate / Paracetamol (Hydrocodone, Bitartrate, Hydrocodo; Gatifloxacin; Zolpidem Tartrate; Lansoprazole; Enoxaparin Sodium (Enoxaparin Sodium, Heparin-Fraction, Sodium Salt); Fentanyl
Adverse event in 60 year old male receiving Promethazine
Reported by a pharmacist from United States on 2007-07-02
Patient: 60 year old male
Adverse reactions / side effects: Vomiting, Nausea, Hypotension, Loss of Consciousness
Adverse event resulted in: life threatening event, hospitalization
Suspect drug(s):
Promethazine
Adverse event in 55 year old female receiving Promethazine
Reported by a pharmacist from United States on 2007-05-25
Patient: 55 year old female, weighing 65.8 kg (144.7 pounds)
Adverse reactions / side effects: Abdominal Pain, Vomiting, Nausea, Fall, Convulsion, Loss of Consciousness, Cardio-Respiratory Arrest, Diarrhoea, Irritable Bowel Syndrome
Adverse event resulted in: life threatening event, hospitalization
Suspect drug(s):
Meperidine HCL
Dosage: 100 mg q3h iv
Indication: Pain
Start date: 2006-10-11
End date: 2006-10-13
Promethazine
Dosage: 25 mg q3h iv
Indication: Nausea
Start date: 2006-10-11
End date: 2006-10-13
Other drugs received by patient: Inderal; Lexapro; Imitrex; Ambien
Adverse event in 35 year old female receiving Promethazine
Reported by a individual with unspecified qualification from United States on 2007-03-08
Patient: 35 year old female, weighing 49.0 kg (107.8 pounds)
Adverse reactions / side effects: Abdominal Pain, Productive Cough, Contusion, Chills, Headache, Pyrexia, Vaginal Haemorrhage, Fatigue, Chest Pain, Thrombocytopenia, Epistaxis, Dyspnoea, Vomiting, Nausea, Haemolytic Anaemia, Leukopenia
Adverse event resulted in: life threatening event, hospitalization
Suspect drug(s):
PEG-Intron
Indication: Hepatitis C
Start date: 2006-04-15
End date: 2006-11-30
Promethazine
Indication: Nausea
Start date: 2006-11-30
Promethazine
Indication: Vomiting
Start date: 2006-11-30
Ribavirin
Administration route: Oral
Indication: Hepatitis C
Start date: 2006-04-15
End date: 2006-11-30
Other drugs received by patient: Synthroid
Adverse event in 70 year old female receiving Promethazine
Reported by a pharmacist from United States on 2007-01-24
Patient: 70 year old female
Adverse reactions / side effects: Cardio-Respiratory Arrest, Convulsion
Adverse event resulted in: life threatening event
Suspect drug(s):
Promethazine
Adverse event in 85 year old female receiving Promethazine
Reported by a pharmacist from United States on 2007-01-04
Patient: 85 year old female, weighing 54.0 kg (118.8 pounds)
Adverse reactions / side effects: Grand MAL Convulsion, Apnoea, Oxygen Saturation Decreased, Loss of Consciousness
Adverse event resulted in: life threatening event, hospitalization, disablity
Suspect drug(s):
Promethazine
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