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Codeine (Codeine) - Side Effect Reports to FDA

 
 



This is an index of side effect / adverse reaction reports (a.k.a. adverse event reports) related to Codeine and submitted to the FDA during the sample period of about a year. The information is not vetted and should not be considered as verified clinical evidence.

Reports by Event Outcome

All Cases (175)
Death (37)
Life Threatening Events (11)
Disability (6)

Reports by Reaction Type

Drug Hypersensitivity (71)Vomiting (17)Toxicity To Various Agents (14)Nausea (13)Pain (11)Abdominal Distension (11)Drug Abuse (10)Cardio-Respiratory Arrest (10)Completed Suicide (9)Dyspnoea (9)Respiratory Arrest (9)Abdominal Pain (8)

Below are a few examples of reports where side effects / adverse reactions may be related to Codeine. For a complete list or a specific selection of reports, please use the links above.

Possible Codeine side effects in male

Reported by a health professional (non-physician/pharmacist) from France on 2012-08-23

Patient: male

Reactions: Intestinal Ischaemia, Abdominal Pain, Abdominal Distension, Intestinal Obstruction

Adverse event resulted in: hospitalization

Drug(s) suspected as cause:
Acetaminophen
    Indication: Product Used FOR Unknown Indication
    Start date: 2012-02-02

Acetaminophen
    Indication: Product Used FOR Unknown Indication

Arixtra
    Indication: Product Used FOR Unknown Indication
    Start date: 2012-03-06
    End date: 2012-03-01

Arixtra
    Start date: 2012-01-27
    End date: 2012-03-01

Atarax
    Dosage: evening
    Indication: Product Used FOR Unknown Indication
    Start date: 2012-03-06

Chlorpromazine HCL
    Indication: Product Used FOR Unknown Indication
    Start date: 2012-01-27

Codeine
    Indication: Product Used FOR Unknown Indication
    Start date: 2012-02-01
    End date: 2012-03-01

Flagyl
    Indication: Product Used FOR Unknown Indication

Imodium
    Start date: 2012-02-02

Imodium
    Indication: Product Used FOR Unknown Indication
    Start date: 2012-03-06
    End date: 2012-03-01

Nexium
    Indication: Product Used FOR Unknown Indication
    Start date: 2012-03-06

Quetiapine Fumarate
    Administration route: Oral
    Indication: Schizophrenia
    Start date: 2012-02-06

Quetiapine Fumarate
    Administration route: Oral
    Start date: 2012-03-06

Rocephin
    Indication: Product Used FOR Unknown Indication

Sandostatin
    Dosage: 1 in the morning and 1 in the evening
    Start date: 2012-03-01
    End date: 2012-03-01

Sandostatin
    Indication: Product Used FOR Unknown Indication
    Start date: 2012-02-01
    End date: 2012-03-01

Spasfon
    Indication: Product Used FOR Unknown Indication
    Start date: 2012-02-02

Tranxene
    Dosage: in the evening
    Indication: Product Used FOR Unknown Indication
    Start date: 2012-03-06

Tranxene
    Start date: 2012-01-27
    End date: 2012-03-01



Possible Codeine side effects in 51 year old female

Reported by a health professional (non-physician/pharmacist) from United States on 2012-08-21

Patient: 51 year old female

Reactions: NO Adverse Event

Drug(s) suspected as cause:
Codeine
    Dosage: unk

Morphine
    Dosage: unk



Possible Codeine side effects in male

Reported by a health professional (non-physician/pharmacist) from France on 2012-08-20

Patient: male

Reactions: Abdominal Pain, Intestinal Ischaemia, Abdominal Distension, Intestinal Obstruction

Adverse event resulted in: hospitalization

Drug(s) suspected as cause:
Acetaminophen
    Indication: Product Used FOR Unknown Indication

Acetaminophen
    Indication: Product Used FOR Unknown Indication
    Start date: 2012-02-02

Arixtra
    Start date: 2012-03-06
    End date: 2012-03-01

Arixtra
    Indication: Product Used FOR Unknown Indication
    Start date: 2012-01-27
    End date: 2012-03-01

Atarax
    Dosage: evening
    Indication: Product Used FOR Unknown Indication
    Start date: 2012-03-06

Chlorpromazine HCL
    Indication: Product Used FOR Unknown Indication
    Start date: 2012-01-27

Codeine
    Indication: Product Used FOR Unknown Indication
    Start date: 2012-02-01
    End date: 2012-03-01

Flagyl
    Indication: Product Used FOR Unknown Indication

Imodium
    Indication: Product Used FOR Unknown Indication
    Start date: 2012-03-06
    End date: 2012-03-01

Imodium
    Start date: 2012-02-02

Nexium
    Indication: Product Used FOR Unknown Indication
    Start date: 2012-03-06

Quetiapine Fumarate
    Administration route: Oral
    Start date: 2012-02-06

Quetiapine Fumarate
    Administration route: Oral
    Indication: Schizophrenia
    Start date: 2012-03-06

Rocephin
    Indication: Product Used FOR Unknown Indication

Sandostatin
    Indication: Product Used FOR Unknown Indication
    Start date: 2012-02-01
    End date: 2012-03-01

Sandostatin
    Dosage: 1 in the morning and 1 in the evening
    Start date: 2012-03-01
    End date: 2012-03-01

Spasfon
    Indication: Product Used FOR Unknown Indication
    Start date: 2012-02-02

Tranxene
    Dosage: in the evening
    Indication: Product Used FOR Unknown Indication
    Start date: 2012-03-06

Tranxene
    Start date: 2012-01-27
    End date: 2012-03-01



Possible Codeine side effects in 75 year old female

Reported by a physician from United States on 2012-08-20

Patient: 75 year old female

Reactions: Drug Hypersensitivity

Drug(s) suspected as cause:
Azithromycin
    Dosage: unk

Codeine

Demerol
    Dosage: unk

Erythromycin

Morphine Sulfate
    Dosage: unk



Possible Codeine side effects in 47 year old female

Reported by a consumer/non-health professional from United States on 2012-08-16

Patient: 47 year old female

Reactions: Drug Hypersensitivity

Drug(s) suspected as cause:
Codeine
    Dosage: unk

Zoloft
    Dosage: unk



Possible Codeine side effects in 55 year old male

Reported by a consumer/non-health professional from United States on 2012-08-13

Patient: 55 year old male, weighing 113.0 kg (248.6 pounds)

Reactions: Off Label Use, Nerve Injury, Pain in Extremity, Oedema Peripheral, Drug Ineffective FOR Unapproved Indication, Pain, Sensory Loss, GUN Shot Wound

Drug(s) suspected as cause:
Codeine
    Dosage: unk
    Indication: Nerve Injury

Lyrica
    Dosage: 400 mg, unk
    Indication: Neuropathy Peripheral
    Start date: 2005-01-01

Lyrica
    Indication: Hypoaesthesia

Lyrica
    Indication: Burning Sensation

Lyrica
    Dosage: 300 mg, 2x/day
    Indication: Pain

Wellbutrin
    Dosage: unk
    Indication: Depression
    Start date: 2005-01-01

Other drugs received by patient: Tramadol



Possible Codeine side effects in 44 year old female

Reported by a physician from United States on 2012-08-13

Patient: 44 year old female, weighing 56.2 kg (123.7 pounds)

Reactions: Drug Hypersensitivity

Drug(s) suspected as cause:
Codeine

Compazine
    Indication: Nausea

Droperidol
    Dosage: unk

Ibuprofen
    Dosage: 200 mg, as needed

Imitrex
    Dosage: unk
    Indication: Migraine

Inapsine

Morphine Sulfate
    Indication: Pain

Motrin
    Dosage: unk

Reglan
    Dosage: unk

Risperdal
    Dosage: unk

Sumatriptan Succinate
    Dosage: unk

Toradol



Possible Codeine side effects in male

Reported by a health professional (non-physician/pharmacist) from Canada on 2012-08-10

Patient: male, weighing 2.9 kg (6.4 pounds)

Reactions: Exposure During Breast Feeding, Respiratory Arrest, Lethargy

Adverse event resulted in: life threatening event, hospitalization

Drug(s) suspected as cause:
Acetaminophen
    Indication: Afterbirth Pain

Codeine
    Dosage: 2.1 mg/kg
    Indication: Pain

Ibuprofen
    Indication: Afterbirth Pain

Oxycodone
    Dosage: every 4 hours for 2 days, and every 6 hours for a subsequent 2 days
    Indication: Afterbirth Pain

Tylenol W / Codeine
    Dosage: 3 df, unk
    Indication: Pain



Possible Codeine side effects in 51 year old female

Reported by a health professional (non-physician/pharmacist) from United States on 2012-08-09

Patient: 51 year old female

Reactions: Drug Hypersensitivity

Drug(s) suspected as cause:
Codeine
    Dosage: unk

Hydrocodone
    Dosage: unk

Morphine Sulfate
    Dosage: unk



Possible Codeine side effects in 49 year old

Reported by a consumer/non-health professional from United States on 2012-08-06

Patient: 49 year old

Reactions: Drug Hypersensitivity, Abdominal Pain Upper

Drug(s) suspected as cause:
Clindamycin Phosphate
    Dosage: unk

Codeine
    Dosage: unk

Darvon
    Dosage: unk



Possible Codeine side effects in female

Reported by a consumer/non-health professional from United States on 2012-08-03

Patient: female, weighing 99.8 kg (219.5 pounds)

Reactions: Hypersensitivity, Sensory Loss, Somnolence, Erythema, Gastric Ulcer, Mania, Fatigue, Balance Disorder, Dizziness, Clumsiness, Anger, Abdominal Distension, Skin Swelling, Psychomotor Hyperactivity, Musculoskeletal Discomfort, Alopecia, Insomnia, Withdrawal Syndrome, Feeling Abnormal

Drug(s) suspected as cause:
Codeine
    Dosage: unk
    Indication: Ehlers-Danlos Syndrome

Gabapentin
    Dosage: 300 mg, 1x/day
    Administration route: Oral
    Indication: Pain
    Start date: 2012-06-18

Gabapentin
    Dosage: 300 mg, 3x/day
    End date: 2012-07-07

Gabapentin
    Dosage: 300 mg, 2x/day
    Start date: 2012-06-01

Ibuprofen
    Dosage: unk
    Indication: Ehlers-Danlos Syndrome

Neurontin
    Dosage: 300 mg, 2x/day
    Start date: 2012-01-01

Neurontin
    Dosage: 300 mg,daily
    Indication: Ehlers-Danlos Syndrome
    Start date: 2012-06-01

Tramadol HCL
    Dosage: unk
    Indication: Ehlers-Danlos Syndrome

Vicodin
    Dosage: unk
    Indication: Ehlers-Danlos Syndrome

Other drugs received by patient: Cyclobenzaprine



Possible Codeine side effects in female

Reported by a physician from United States on 2012-08-02

Patient: female

Reactions: Drug Hypersensitivity

Drug(s) suspected as cause:
Codeine
    Dosage: unk

Lipitor
    Dosage: unk



Possible Codeine side effects in

Reported by a health professional (non-physician/pharmacist) from United States on 2012-08-02

Patient:

Reactions: Drug Hypersensitivity

Drug(s) suspected as cause:
Amoxicillin

Codeine

Crestor

Enalapril Maleate
    Dosage: unk
    Administration route: Oral

Fosamax
    Dosage: unk
    Administration route: Oral

Klonopin

Neurontin

Penicillin G Potassium

Pravastatin Sodium

Procardia

Zocor
    Dosage: unk
    Administration route: Oral



Possible Codeine side effects in 29 year old female

Reported by a consumer/non-health professional from United States on 2012-08-01

Patient: 29 year old female, weighing 99.8 kg (219.5 pounds)

Reactions: Hypersensitivity, Sensory Loss, Erythema, Somnolence, Gastric Ulcer, Mania, Arthropathy, Fatigue, Balance Disorder, Clumsiness, Dizziness, Abdominal Distension, Anger, Skin Swelling, Psychomotor Hyperactivity, Abnormal Behaviour, Insomnia, Alopecia, Withdrawal Syndrome

Drug(s) suspected as cause:
Codeine
    Indication: Ehlers-Danlos Syndrome

Ibuprofen
    Indication: Ehlers-Danlos Syndrome

Neurontin
    Dosage: two times a day
    Administration route: Oral
    Start date: 2012-01-01
    End date: 2012-01-01

Neurontin
    Dosage: thrice daily
    Administration route: Oral
    Indication: Ehlers-Danlos Syndrome
    End date: 2012-07-07

Neurontin
    Dosage: daily
    Administration route: Oral
    Start date: 2012-06-01
    End date: 2012-01-01

Neurontin
    Dosage: daily
    Administration route: Oral
    Start date: 2012-06-18

Neurontin
    Dosage: two times a day
    Administration route: Oral
    Start date: 2012-06-01

NON Steroidal Anti-Inflammatory Drugs
    Indication: Ehlers-Danlos Syndrome

Tramadol Hydrochloride
    Indication: Ehlers-Danlos Syndrome

Vicodin
    Indication: Ehlers-Danlos Syndrome

Other drugs received by patient: Cyclobenzaprine



Possible Codeine side effects in

Reported by a health professional (non-physician/pharmacist) from United States on 2012-08-01

Patient:

Reactions: Back Pain, Dyspnoea, HIP Arthroplasty, Vomiting, Nausea, Abasia, Drug Hypersensitivity, Constipation, Skin Irritation, Myalgia, Fatigue, Sleep Disorder, Asthenia, Blood Glucose Increased

Adverse event resulted in: disablity

Drug(s) suspected as cause:
Alprazolam

Codeine

Coreg

Cyclosporine

Glucophage

Ibuprofen (Advil)
    Dosage: 200 mg, prn

Lipitor

Lotrimin

Luvox

Metformin Hydrochloride
    Dosage: 500 mg, unk

Metoprolol Tartrate
    Dosage: 25 mg, bid

Motrin

Plavix

Proscar
    Administration route: Oral

Prozac

Reglan

Toprol-XL

Tramadol Hydrochloride

Viagra

Xalatan

Zetia
    Administration route: Oral

Zocor
    Administration route: Oral

Other drugs received by patient: Folic Acid; Pilocarpine; Timolol Maleate; Lantus; Lumigan; Pravastatin Sodium; Thera Tears; Potassium Chloride - USP; Vicodin; Digoxin; Aspirin; Diazepam; Furosemide; Cozaar; Bilberry; Oxycodone HCL; Aspirin; Omega-3 Marine Triglycerides; Clozapine; Allopurinol



Possible Codeine side effects in

Reported by a health professional (non-physician/pharmacist) from United States on 2012-07-31

Patient:

Reactions: Back Pain, Dyspnoea, Vomiting, Nausea, Abasia, Constipation, Skin Irritation, Myalgia, Fatigue, Sleep Disorder, Asthenia, Blood Glucose Increased

Adverse event resulted in: hospitalization, disablity

Drug(s) suspected as cause:
Alprazolam

Clozapine

Codeine

Coreg

Cyclosporine

Glucophage

Ibuprofen (Advil)

Lipitor

Lotrimin AF

Lumigan

Luvox

Metformin Hydrochloride
    Dosage: 500 mg, unk

Metoprolol Tartrate
    Dosage: 25 mg, bid
    Administration route: Oral

Motrin

Oxycodone HCL

Plavix

Pravastatin Sodium

Proscar
    Administration route: Oral

Prozac

Reglan

Toprol-XL

Tramadol Hydrochloride

Viagra

Vicodin

Xalatan
    Dosage: 200 mg, prn

Zetia
    Administration route: Oral

Zocor
    Administration route: Oral

Other drugs received by patient: Losartan Potassium; Thera Tears; Folic Acid; Digoxin; Bilberry; Omega-3 Marine Triglycerides; Pilocarpine; Furosemide; Diazepam; Istalol; Lantus; Allopurinol; Potassium Chloride; Aspirin



Possible Codeine side effects in

Reported by a health professional (non-physician/pharmacist) from United States on 2012-07-31

Patient:

Reactions: Back Pain, Vomiting, Dyspnoea, HIP Arthroplasty, Nausea, Abasia, Drug Hypersensitivity, Constipation, Skin Irritation, Myalgia, Fatigue, Sleep Disorder, Asthenia, Blood Glucose Increased

Adverse event resulted in: disablity

Drug(s) suspected as cause:
Alprazolam

Codeine

Coreg

Cyclosporine

Glucophage

Ibuprofen (Advil)
    Dosage: unk, prn

Lipitor

Lotrimin

Luvox

Metformin Hydrochloride

Metoprolol Tartrate
    Dosage: unk, qd

Motrin

Motrin
    Dosage: unk, prn

Plavix

Proscar
    Administration route: Oral

Prozac

Reglan

Toprol-XL

Tramadol Hydrochloride

Viagra

Xalatan

Zetia
    Administration route: Oral

Zocor
    Administration route: Oral

Other drugs received by patient: Timolol Maleate; Thera Tears; Clozapine; Omega-3 Marine Triglycerides; Aspirin; Losartan Potassium; Allopurinol; Lantus; Potassium Chloride; Pravastatin Sodium; Digoxin; Diazepam; Bilberry; Lumigan; Folic Acid; Furosemide; Oxycodone HCL; Pilocarpine; Acetaminophen / Hydrocodone Bitartrate



Possible Codeine side effects in female

Reported by a health professional (non-physician/pharmacist) from United States on 2012-07-31

Patient: female

Reactions: Drug Hypersensitivity, Allergy To Chemicals

Drug(s) suspected as cause:
Celebrex
    Dosage: unk
    Indication: Arthritis

Clindamycin HCL
    Dosage: unk

Codeine
    Dosage: unk

Darvocet
    Dosage: unk

Demerol
    Dosage: unk

Diazepam
    Dosage: 10 mg, unk

Ibuprofen
    Dosage: unk

Macrodantin
    Dosage: unk



Possible Codeine side effects in female

Reported by a consumer/non-health professional from United States on 2012-07-30

Patient: female

Reactions: Drug Hypersensitivity

Drug(s) suspected as cause:
Aspirin
    Dosage: unk

Codeine
    Dosage: unk

Ibuprofen
    Dosage: unk



Possible Codeine side effects in female

Reported by a consumer/non-health professional from United States on 2012-07-25

Patient: female

Reactions: Drug Hypersensitivity

Drug(s) suspected as cause:
Codeine
    Dosage: unk

Reglan
    Dosage: unk

Valium
    Dosage: unk

Vibramycin
    Dosage: unk



Possible Codeine side effects in female

Reported by a physician from United States on 2012-07-24

Patient: female

Reactions: Drug Hypersensitivity

Drug(s) suspected as cause:
Codeine
    Dosage: unk

Oxycodone Hydrochloride
    Dosage: unk



Possible Codeine side effects in female

Reported by a health professional (non-physician/pharmacist) from United States on 2012-07-24

Patient: female

Reactions: Drug Hypersensitivity

Drug(s) suspected as cause:
Codeine
    Dosage: unk

Morphine Sulfate
    Dosage: unk



Possible Codeine side effects in 29 year old female

Reported by a consumer/non-health professional from United States on 2012-07-17

Patient: 29 year old female, weighing 100.0 kg (220.0 pounds)

Reactions: Hypersensitivity, Psychomotor Hyperactivity, Abnormal Behaviour, Gastric Ulcer, Mania, Balance Disorder, Alopecia, Insomnia, Clumsiness, Abdominal Distension, Dizziness

Drug(s) suspected as cause:
Codeine
    Indication: Ehlers-Danlos Syndrome

Ibuprofen
    Indication: Ehlers-Danlos Syndrome

Neurontin
    Dosage: daily
    Indication: Ehlers-Danlos Syndrome
    Start date: 2012-01-01

Neurontin
    Dosage: daily
    Start date: 2012-06-01
    End date: 2012-01-01

Neurontin
    Dosage: two times a day
    Start date: 2012-01-01
    End date: 2012-01-01

NON Steroidal Anti-Inflammatory Drugs
    Indication: Ehlers-Danlos Syndrome

Tramadol HCL
    Indication: Ehlers-Danlos Syndrome

Vicodin
    Indication: Ehlers-Danlos Syndrome

Other drugs received by patient: Cyclobenazprine



Possible Codeine side effects in female

Reported by a consumer/non-health professional from United States on 2012-07-17

Patient: female, weighing 84.8 kg (186.6 pounds)

Reactions: Diverticulitis, Tachycardia, Tricuspid Valve Incompetence, Chronic Obstructive Pulmonary Disease, Cardiomegaly, Iron Deficiency Anaemia, Oedema Peripheral, Pneumonitis, Ventricular Extrasystoles, Back Pain, Bartholin's Cyst, Left Ventricular Hypertrophy, Bursitis, Osteitis, Emotional Distress, Temporomandibular Joint Syndrome, Oral Fibroma, Ocular Hyperaemia, Aortic Valve Disease, Rectal Haemorrhage, Occipital Neuralgia, Hypercholesterolaemia, Vitreous Floaters, Abdominal Distension, Depression, Bone Disorder, Exostosis, Emphysema, Fluid Overload, Tooth Fracture, Bone Giant Cell Tumour, Gout, Haemorrhoids, Febrile Neutropenia, Electrocardiogram QRS Complex Abnormal, Arthralgia, Life Expectancy Shortened, Sepsis, Atrioventricular Block, Primary Sequestrum, Aortic Stenosis, Osteomyelitis, Clostridium Difficile Colitis, Herpes Zoster, Arthropathy, Hypoxia, Irritable Bowel Syndrome, Carpal Tunnel Syndrome, Cardiac Failure Congestive, Intervertebral Disc Protrusion, Actinic Keratosis, Cardiac Murmur, Hiatus Hernia, Chest Discomfort, Pneumonia, General Physical Health Deterioration, Decreased Interest, Mitral Valve Calcification, Osteosclerosis, Excessive Granulation Tissue, Synovial Rupture, Tooth Abscess, Mouth Ulceration, Pain, Petechiae, Neoplasm Progression, Synovial Cyst, Laryngitis, Dyspnoea Exertional, Neuropathy Peripheral, Interstitial Lung Disease, Chronic Sinusitis, Pleural Effusion, Toothache, Pyuria, Hallucination, Spinal Deformity, Electrocardiogram T Wave Inversion, Pharyngitis, Engraftment Syndrome, Migraine, Type 2 Diabetes Mellitus, Sympathetic Posterior Cervical Syndrome, Dental Caries, Drug Hypersensitivity, Atrial Fibrillation, Osteolysis, Deformity, Pulmonary Fibrosis, Osteoarthritis, Anxiety, Osteonecrosis of JAW, Bronchiectasis, Neoplasm Malignant, Ejection Fraction Decreased, Hypophagia, Oral Disorder, Spinal Osteoarthritis, Blindness, Infection

Adverse event resulted in: hospitalization

Drug(s) suspected as cause:
Aredia
    Indication: Multiple Myeloma
    End date: 2006-01-01

Biotin

Codeine

Zometa
    Indication: Multiple Myeloma

Other drugs received by patient: Synthroid; CAL-MAG; Premarin; Bortezomib; Acyclovir; Altace; Hydrochlorothiazide; Imdur; Versed; Losartan Potassium; Amoxicillin; Furosemide; Selenium; Fentanyl; Vancomycin; Gabapentin; Magnesium Sulfate; Aspirin; Lasix; Crocin; Chromium Chloride; Zestril; Warfarin Sodium; Crestor; Imodium; Zinc Sulfate; Multi-Vitamins; Xanax; Januvia; Alprazolam; Potassium Chloride; Claritin; Phenergan; Decadron; Revlimid



Possible Codeine side effects in female

Reported by a health professional (non-physician/pharmacist) from United States on 2012-07-13

Patient: female

Reactions: Drug Hypersensitivity, Allergy To Chemicals

Drug(s) suspected as cause:
Celebrex
    Dosage: unk
    Indication: Arthritis

Clindamycin HCL
    Dosage: unk

Codeine
    Dosage: unk

Darvocet
    Dosage: unk

Demerol
    Dosage: unk

Diazepam
    Dosage: 10 mg, unk

Ibuprofen
    Dosage: unk

Macrodantin
    Dosage: unk



Possible Codeine side effects in female

Reported by a consumer/non-health professional from United States on 2012-07-11

Patient: female, weighing 100.0 kg (220.0 pounds)

Reactions: Hypersensitivity, Psychomotor Hyperactivity, Gastric Ulcer, Mania, Balance Disorder, Insomnia, Alopecia, Clumsiness, Dizziness, Abdominal Distension, Feeling Abnormal

Drug(s) suspected as cause:
Codeine
    Dosage: unk
    Indication: Ehlers-Danlos Syndrome

Ibuprofen
    Dosage: unk
    Indication: Ehlers-Danlos Syndrome

Neurontin
    Dosage: 300 mg,daily
    Indication: Ehlers-Danlos Syndrome
    Start date: 2012-06-01

Tramadol HCL
    Dosage: unk
    Indication: Ehlers-Danlos Syndrome

Vicodin
    Dosage: unk
    Indication: Ehlers-Danlos Syndrome

Other drugs received by patient: Cyclobenzaprine



Possible Codeine side effects in

Reported by a individual with unspecified qualification from Australia on 2012-06-27

Patient:

Reactions: Death, Foreign Body Reaction, Toxicity To Various Agents, Drug Abuse

Adverse event resulted in: death

Drug(s) suspected as cause:
Codeine
    Dosage: unk, unknown
    Indication: Product Used FOR Unknown Indication

Diazepam
    Dosage: unk, unknown
    Indication: Product Used FOR Unknown Indication

Heroin
    Dosage: unk, unknown
    Indication: Product Used FOR Unknown Indication

Morphine
    Dosage: unk, unknown
    Indication: Product Used FOR Unknown Indication

Oxazepam
    Dosage: unk, unknown
    Indication: Product Used FOR Unknown Indication

Temazepam
    Dosage: unk, unknown
    Indication: Product Used FOR Unknown Indication



Possible Codeine side effects in 35 year old

Reported by a health professional (non-physician/pharmacist) from Australia on 2012-06-27

Patient: 35 year old

Reactions: Accidental Poisoning, Toxicity To Various Agents, Accidental Overdose, Arrhythmia

Adverse event resulted in: death

Drug(s) suspected as cause:
Acetaminophen
    Dosage: unk
    Indication: Product Used FOR Unknown Indication

Codeine
    Dosage: unk
    Indication: Product Used FOR Unknown Indication

Ibruprofen
    Dosage: unk
    Indication: Product Used FOR Unknown Indication

Ibuprofen
    Dosage: unk
    Indication: Product Used FOR Unknown Indication

Methadone HCL
    Dosage: unk
    Indication: Product Used FOR Unknown Indication

Methamphetamine Hydrochloride
    Dosage: unk
    Indication: Product Used FOR Unknown Indication



Possible Codeine side effects in

Reported by a health professional (non-physician/pharmacist) from Canada on 2012-06-20

Patient:

Reactions: Maternal Exposure During Pregnancy, Kidney Malformation

Drug(s) suspected as cause:
Acetaminophen

Citalopram Hydrobromide

Clotrimazole

Codeine

Diphenhydramine HCL
    Indication: Hyperemesis Gravidarum

Domperidone

Ginger

Glycerol 2.6%

Hydromorphone HCL
    Indication: Pain

Hydroxyzine

Indomethacin

Lactulose

Methylprednisolone

Metoclopramide
    Dosage: 1.8-3.2 mg/h
    Indication: Hyperemesis Gravidarum

Omeprazole

Ondansetron
    Indication: Hyperemesis Gravidarum

Pantoprazole

Prednisone TAB

Ranitidine

Sodium Dioctyl Sulfosuccinate



Possible Codeine side effects in 52 year old female

Reported by a individual with unspecified qualification from Canada on 2012-06-20

Patient: 52 year old female

Reactions: Drug Hypersensitivity, Crohn's Disease, Hypotension, Anaphylactic Shock, Drug Interaction, Cystitis, Disease Progression, Abdominal Discomfort, Dehydration, Incision Site Abscess, Dizziness, Abdominal Distension, Bladder Operation, White Blood Cell Count Increased

Adverse event resulted in: life threatening event, hospitalization

Drug(s) suspected as cause:
Amoxicillin
    Indication: Cystitis
    Start date: 2010-08-01

Avelox
    Indication: Cystitis
    Start date: 2010-08-01

Codeine
    Indication: Product Used FOR Unknown Indication
    Start date: 2010-08-01

Cotrim
    Indication: Cystitis

Remicade
    Dosage: 1 every 8 week(s)
    Indication: Crohn's Disease
    Start date: 2009-07-01

Remicade

Remicade
    Start date: 2010-09-13

Remicade
    Start date: 2010-09-13

Remicade
    Dosage: 1 every 8 week(s)

Other drugs received by patient possibly interacting with the suspect drug:
Macrobid
    Indication: Crohn's Disease
    Start date: 2010-08-01

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