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Morphine (Morphine) - Reports of Side Effects & Adverse Reactions

 



This is an index of reports of adverse events (side effects, adverse reactions, etc.) related to Morphine. 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 (263)
     Drug Ineffective (19)Overdose (19)Vomiting (18)more >>

Cases resulting in a serious event (247)
     Drug Ineffective (19)Overdose (18)Diarrhoea (18)more >>

Cases resulting in death (62)
     Completed Suicide (15)Drug Toxicity (9)Overdose (8)more >>

Cases resulting in life threatening events (32)
     Loss of Consciousness (8)Hypotension (6)Respiratory Failure (6)more >>

Cases resulting in hospitalization (115)
     Confusional State (15)Constipation (13)Unresponsive TO Stimuli (10)more >>

Cases resulting in disability (15)
     Enthesopathy (6)Constipation (6)Diarrhoea (6)more >>

Cases resulting in other serious reactions (114)
     Drug Ineffective (12)Overdose (10)Respiratory Arrest (10)more >>

Below is a sample of reports where side effects / adverse reactions may be related to Morphine. For a complete list and/or a specific selection of reports, please use the links in the index above.

Adverse event in female receiving Morphine

Reported by a consumer/non-health professional from France on 2007-10-31

Patient: female, weighing 0.8 kg (1.8 pounds)

Adverse reactions / side effects: Myoclonus

Adverse event resulted in: disablity

Suspect drug(s):
Fortum
    Dosage: 25mg three times per day
    Indication: Infection
    Start date: 2007-07-01
    End date: 2007-07-01

Morphine
    Dosage: 10mck see dosage text
    Indication: Pain
    Start date: 2007-07-01
    End date: 2007-07-03

Triflucan
    Dosage: 2.8mg per day
    Indication: Infection
    Start date: 2007-07-01
    End date: 2007-07-01

Vancomycin
    Dosage: 11mg per day
    Indication: Infection
    Start date: 2007-07-01
    End date: 2007-07-03



Adverse event in 76 year old female receiving Morphine

Reported by a individual with unspecified qualification on 2007-10-31

Patient: 76 year old female

Adverse reactions / side effects: Bradypnoea, Miosis, Unresponsive TO Stimuli, Coma, Corneal Reflex Decreased

Adverse event resulted in: life threatening event

Suspect drug(s):
Morphine
    Dosage: 1/2 vial
    Indication: Pain

Oxycontin
    Dosage: 20 mg, bid
    Administration route: Oral
    Indication: Pain



Adverse event in 51 year old receiving Morphine

Reported by a physician from United States on 2007-10-31

Patient: 51 year old

Adverse reactions / side effects: Completed Suicide, Respiratory Arrest, Cardiac Arrest

Adverse event resulted in: death

Suspect drug(s):
Diazepam
    Dosage: acute exposure.
    Administration route: Oral
    Indication: Drug USE FOR Unknown Indication

Morphine
    Dosage: acute exposure.
    Administration route: Oral
    Indication: Drug USE FOR Unknown Indication

Tricyclic Antidepressant NOS
    Dosage: acute exposure.
    Administration route: Oral
    Indication: Drug USE FOR Unknown Indication



Adverse event in 53 year old female receiving Morphine

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 male receiving Morphine

Reported by a individual with unspecified qualification on 2007-10-30

Patient: male

Adverse reactions / side effects: Renal Failure, Medication Error, Coma

Adverse event resulted in: life threatening event

Suspect drug(s):
Morphine



Adverse event in 82 year old female receiving Morphine

Reported by a individual with unspecified qualification on 2007-10-30

Patient: 82 year old female

Adverse reactions / side effects: Haemoglobin Decreased, Cardiac Failure, Dizziness

Suspect drug(s):
Morphine
    Indication: Procedural Pain

Morphine

Naloxone
    Dosage: 0,25 mcg/kg/h
    Indication: Procedural Pain

Tramacet
    Dosage: 2 tablets preoperatively and then 6-hourly
    Administration route: Oral
    Indication: Procedural Pain

Other drugs received by patient: Bupivacaine; Ropivacaine; Ketorolac; Celebrex



Adverse event in 47 year old male receiving Morphine

Reported by a individual with unspecified qualification from United Kingdom on 2007-10-29

Patient: 47 year old male

Adverse reactions / side effects: Blood Alcohol Increased, Drug Level Above Therapeutic, Drug Toxicity, Drug Interaction Potentiation, Drug Abuse

Adverse event resulted in: death

Suspect drug(s):
Benzodiapines(no Ingredients / Substances)

Codeine Phosphate (Ngx)(codeine Phosphate) Unknown

Ethanol(ethanol)

Heminevrin(clomethiazole Edisilate)
    Dosage: oral
    Administration route: Oral

Morphine

Opium Derivatives and Expectorants(no Ingredients / Substances)



Adverse event in 47 year old receiving Morphine

Reported by a physician from United States on 2007-10-29

Patient: 47 year old

Adverse reactions / side effects: Death, Drug Toxicity, Completed Suicide, Respiratory Arrest, Cardiac Arrest

Adverse event resulted in: death

Suspect drug(s):
Diazepam
    Indication: Drug USE FOR Unknown Indication

Morphine
    Indication: Drug USE FOR Unknown Indication



Adverse event in 35 year old receiving Morphine

Reported by a physician from United States on 2007-10-29

Patient: 35 year old

Adverse reactions / side effects: Completed Suicide, Respiratory Arrest, Cardiac Arrest

Adverse event resulted in: death

Suspect drug(s):
Clonazepam
    Dosage: acute exposure. route: ingestion.
    Administration route: Oral
    Indication: Drug USE FOR Unknown Indication

Insulin
    Dosage: acute exposure. route: ingestion.
    Administration route: Oral
    Indication: Drug USE FOR Unknown Indication

Morphine
    Dosage: acute exposure. route: ingestion.
    Administration route: Oral
    Indication: Drug USE FOR Unknown Indication

Unspecified Drugs
    Indication: Drug USE FOR Unknown Indication



Adverse event in 51 year old receiving Morphine

Reported by a physician from United States on 2007-10-26

Patient: 51 year old

Adverse reactions / side effects: Completed Suicide, Respiratory Arrest, Cardiac Arrest

Adverse event resulted in: death

Suspect drug(s):
Diazepam
    Dosage: acute exposure.
    Administration route: Oral
    Indication: Drug USE FOR Unknown Indication

Morphine
    Dosage: acute exposure.
    Administration route: Oral
    Indication: Drug USE FOR Unknown Indication

Tricyclic Antidepressant NOS
    Dosage: acute exposure.
    Administration route: Oral
    Indication: Drug USE FOR Unknown Indication



Adverse event in female receiving Morphine

Reported by a individual with unspecified qualification from United States on 2007-10-26

Patient: female, weighing 74.8 kg (164.6 pounds)

Adverse reactions / side effects: Anaemia, Pancytopenia, Narcotic Intoxication, Neutropenia

Adverse event resulted in: hospitalization

Suspect drug(s):
Cetuximab

Darbepoetin Alfa
    Indication: Anaemia of Malignant Disease
    Start date: 2007-02-26
    End date: 2007-04-10

Epoetin Alfa
    Dosage: text:500 ug-freq:frequency: 1 in 3 week
    Indication: Anaemia of Malignant Disease
    Start date: 2007-02-26
    End date: 2007-04-10

Irinotecan HCL

Morphine

Other drugs received by patient: Zofran



Adverse event in 53 year old receiving Morphine

Reported by a physician from United States on 2007-10-26

Patient: 53 year old

Adverse reactions / side effects: Death

Adverse event resulted in: death

Suspect drug(s):
Diazepam
    Administration route: Oral
    Indication: Drug USE FOR Unknown Indication

Hydrocodone Bitartrate and Acetaminophen
    Dosage: drug name reported as acetaminophen/hydrocodone.
    Administration route: Oral
    Indication: Drug USE FOR Unknown Indication

Morphine
    Dosage: (long-active) treatment.
    Administration route: Oral
    Indication: Drug USE FOR Unknown Indication

Unspecified Drugs
    Indication: Drug USE FOR Unknown Indication



Adverse event in receiving Morphine

Reported by a physician from United States on 2007-10-26

Patient:

Adverse reactions / side effects: Death, Respiratory Arrest, Cardiac Arrest

Adverse event resulted in: death

Suspect drug(s):
Diazepam
    Dosage: route reported as ingestion.
    Administration route: Oral
    Indication: Drug USE FOR Unknown Indication

Morphine
    Dosage: route reported as ingestion.
    Administration route: Oral
    Indication: Drug USE FOR Unknown Indication



Adverse event in 55 year old female receiving Morphine

Reported by a individual with unspecified qualification from United States on 2007-10-25

Patient: 55 year old female, weighing 83.0 kg (182.6 pounds)

Adverse reactions / side effects: Pruritus, Infusion Related Reaction

Suspect drug(s):
Morphine



Adverse event in 51 year old receiving Morphine

Reported by a physician from United States on 2007-10-25

Patient: 51 year old

Adverse reactions / side effects: Completed Suicide

Adverse event resulted in: death

Suspect drug(s):
Diazepam
    Dosage: acute exposure.
    Administration route: Oral
    Indication: Drug USE FOR Unknown Indication

Morphine
    Dosage: acute exposure.
    Administration route: Oral
    Indication: Drug USE FOR Unknown Indication

Tricyclic Antidepressant NOS
    Dosage: acute exposure.
    Administration route: Oral
    Indication: Drug USE FOR Unknown Indication



Adverse event in male receiving Morphine

Reported by a health professional (non-physician/pharmacist) from United States on 2007-10-24

Patient: male, weighing 64.7 kg (142.3 pounds)

Adverse reactions / side effects: Metabolic Acidosis, Nausea, Hypotension, Tachycardia, Renal Impairment, Diarrhoea, Intestinal Infarction, Leukopenia

Adverse event resulted in: death

Suspect drug(s):
Compazine
    Dosage: 10 mg prn oral
    Administration route: Oral
    Indication: Nausea

Coumadin
    Dosage: 2.5 mg daily oral
    Administration route: Oral

Cozaar
    Dosage: 50 mg daily oral
    Administration route: Oral
    Indication: Hypertension

Duragesic-25
    Dosage: 25 mcg q three days derm
    Indication: Pain

Iressa
    Dosage: 250 mg daily oral
    Administration route: Oral
    Start date: 2007-09-17
    End date: 2007-10-18

Klonopin
    Dosage: 1 mg prn oral
    Administration route: Oral
    Indication: Somnolence

Morphine
    Dosage: 1 tsp q 2-4 hrns prn oral
    Administration route: Oral
    Indication: Pain

Viagra
    Dosage: 50 mg prn oral
    Administration route: Oral



Adverse event in 47 year old male receiving Morphine

Reported by a individual with unspecified qualification from United Kingdom on 2007-10-24

Patient: 47 year old male

Adverse reactions / side effects: Drug Toxicity, Blood Ethanol Increased, Drug Level Increased, Drug Abuser, Drug Interaction, Respiratory Depression

Adverse event resulted in: death

Suspect drug(s):
Benzodiazepines(no Ingredients / Substances)

Codeine Phosphate (Ngx)(codeine Phosphate) Unknown

Ethanol(ethanol)

Heminevrin(clomethiazole Edisilate)
    Dosage: oral
    Administration route: Oral

Morphine

Opium Derivatives and Expectorants(no Ingredients / Substances)



Adverse event in male receiving Morphine

Reported by a consumer/non-health professional from United Kingdom on 2007-10-23

Patient: male

Adverse reactions / side effects: Death

Adverse event resulted in: death

Suspect drug(s):
Acetaminophen
    Dosage: 4000 mg, qd
    Indication: Pain
    Start date: 2007-08-08

Acetaminophen
    Dosage: 1000 mg, prn
    Administration route: Oral
    Start date: 2007-08-08
    End date: 2007-08-08

Bevacizumab
    Dosage: 450 mg, q2w
    Indication: Gastric Cancer
    Start date: 2007-06-13

Duragesic-100
    Dosage: 125 a?g, qd
    Indication: Pain
    Start date: 2007-08-01

Duragesic-100
    Dosage: 100 a?g, qd
    Start date: 2007-06-13
    End date: 2007-08-01

Duragesic-100
    Dosage: 75 a?g, qd
    Start date: 2007-06-07
    End date: 2007-06-13

Duragesic-100
    Dosage: 50 a?g, qd
    End date: 2007-06-07

Erlotinib
    Dosage: 150 mg, qd
    Administration route: Oral
    Indication: Gastric Cancer
    Start date: 2007-06-13

Gabapentin
    Dosage: 900 mg, qd
    Administration route: Oral
    Indication: Pain
    Start date: 2007-08-08
    End date: 2007-08-13

Gabapentin
    Dosage: 1800 mg, qd
    Administration route: Oral
    End date: 2007-08-08

Imodium
    Dosage: 1 mg, prn
    Administration route: Oral
    Indication: Diarrhoea
    Start date: 2007-06-27

Metadon
    Dosage: 90 mg, qd
    Administration route: Oral
    Indication: Pain

Morphine
    Dosage: 30 mg, prn
    Administration route: Oral
    Indication: Pain

Prednisolone
    Dosage: 25 mg, qd
    Administration route: Oral
    Indication: Nausea
    Start date: 2007-07-10

Supplement NOS
    Administration route: Oral
    Indication: Weight Decreased
    Start date: 2007-06-27



Adverse event in male receiving Morphine

Reported by a health professional (non-physician/pharmacist) from United States on 2007-10-23

Patient: male, weighing 87.5 kg (192.5 pounds)

Adverse reactions / side effects: Osteonecrosis, Pneumonia, Haemoptysis, Tooth Disorder

Adverse event resulted in: hospitalization

Suspect drug(s):
Ativan
    Dosage: 0.5 mg q 8 hr prn oral
    Administration route: Oral

Compazine
    Dosage: 10 mg q 6 hours prn oral
    Administration route: Oral
    Indication: Nausea

Duragesic-100
    Dosage: 25 mcg q 3 days derm
    Indication: Pain

Iressa
    Dosage: 250 mg once daily oral
    Administration route: Oral
    Start date: 2007-02-19
    End date: 2007-10-09

Morphine
    Dosage: 1 tsp prn oral
    Administration route: Oral
    Indication: Breakthrough Pain

Neurontin
    Dosage: 300 mg bid oral
    Administration route: Oral

Novolin 70 / 30
    Dosage: 20 units q 8 hr sq

Plavix
    Dosage: 75 mg qd oral
    Administration route: Oral

Zoloft
    Dosage: 50 mg 2 tab hs oral
    Administration route: Oral



Adverse event in 11 year old male receiving Morphine

Reported by a physician from United States on 2007-10-22

Patient: 11 year old male, weighing 45.0 kg (99.0 pounds)

Adverse reactions / side effects: Vomiting, Blood PH Decreased, Blood Potassium Increased, Blood Bicarbonate Decreased, Blood Creatine Increased, Loss of Consciousness, Overdose, Aspiration, Cardiac Arrest, White Blood Cell Count Increased, Blood Glucose Increased

Adverse event resulted in: death

Suspect drug(s):
Atropine
    Dosage: unspecified

Benadryl
    Dosage: unspecified
    Indication: Dermatitis Contact

Codeine SUL TAB
    Dosage: unspecified

Diazepam
    Dosage: unspecified

Morphine
    Dosage: unspecified

Oxazepam
    Dosage: unspecified

Phenergan
    Dosage: unspecified, rectal
    Indication: Vomiting



Adverse event in 30 year old female receiving Morphine

Reported by a individual with unspecified qualification on 2007-10-18

Patient: 30 year old female, weighing 72.0 kg (158.4 pounds)

Adverse reactions / side effects: Face Oedema, Psoriasis, Pyrexia, Somnolence, Generalised Oedema

Suspect drug(s):
Chlorpheniramine TAB
    Indication: Pruritus

Gentamicin

Metronidazole

Morphine
    Administration route: Oral
    Indication: Pain

Paracetamol
    Indication: Pain

Other drugs received by patient: Dexamethasone 0.5mg TAB; Cyclosporine; Compound Sodium Lactate



Adverse event in 34 year old female receiving Morphine

Reported by a pharmacist from United States on 2007-10-18

Patient: 34 year old female, weighing 75.0 kg (165.0 pounds)

Adverse reactions / side effects: Confusional State, Wrong Drug Administered, Mental Status Changes

Adverse event resulted in: hospitalization

Suspect drug(s):
Morphine

Other drugs received by patient: Metoprolol; Enalapril Maleate; Aspirin; VIT C; Cefazolin; Klonopin; Temazepam; Prednisone; Cellcept; Metoclopramide; Ritalin



Adverse event in 43 year old male receiving Morphine

Reported by a health professional (non-physician/pharmacist) from United States on 2007-10-18

Patient: 43 year old male

Adverse reactions / side effects: Incoherent, Overdose, Eye Rolling, Asthenia

Suspect drug(s):
Aleve
    End date: 2007-01-01

Morphine
    Dosage: topical
    Administration route: Topical
    End date: 2007-01-01

Neurontin
    End date: 2007-01-01

Oxycodone HCL
    End date: 2007-01-01

Rebif
    Dosage: 44 mcg (3 in 1 wk), subcutaneous
    Indication: Multiple Sclerosis
    Start date: 2006-10-03

Vicodin



Adverse event in female receiving Morphine

Reported by a individual with unspecified qualification on 2007-10-18

Patient: female

Adverse reactions / side effects: Premature Baby

Suspect drug(s):
Chlorpheniramine TAB

Compound Sodium Lactate

Cyclosporine

Dexamethasone 0.5mg TAB
    Indication: Maternal Therapy TO Enhance Foetal Lung Maturity

Gentamicin

Metronidazole

Morphine

Paracetamol



Adverse event in 14 month old male receiving Morphine

Reported by a consumer/non-health professional from United States on 2007-10-18

Patient: 14 month old male

Adverse reactions / side effects: Overdose, Unresponsive TO Stimuli

Adverse event resulted in: death

Suspect drug(s):
Heroin (Diamorphine)
    Indication: Drug USE FOR Unknown Indication

Hydromorphone HCL
    Indication: Drug USE FOR Unknown Indication

Morphine
    Indication: Drug USE FOR Unknown Indication

Olanzapine
    Indication: Drug USE FOR Unknown Indication

Oxycodone HCL
    Indication: Drug USE FOR Unknown Indication

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