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Index of reports
> Cases resulting in other serious reactions (14)
> Cases with Pruritus (3)
Below is the selection of adverse event reports related to Lortab (Hydrocodone / Acetaminophen) that includes cases resulting in other serious reactions where reactions include pruritus.
Adverse event in female receiving Lortab (Hydrocodone / Acetaminophen)
Reported by a consumer/non-health professional from United States on 2007-07-24
Patient: female, weighing 52.2 kg (114.8 pounds)
Adverse reactions / side effects: Night Sweats, Pruritus, Head Injury, Urticaria, Pain, Flatulence, Disorientation, Constipation, Somnolence, Loss of Consciousness, Feeling Cold, Weight Increased, Abnormal Dreams, Medication Error, Chest Pain, Abdominal Distension, Depression, Nightmare, Dyspnoea, Chest Discomfort, Vomiting, Nausea, Pain in Extremity, Musculoskeletal Pain, Hypoaesthesia, Dysgeusia, Insomnia, Eye Swelling, Blood Pressure Decreased
Suspect drug(s):
Avalide
Chantix
Administration route: Oral
Indication: Smoking Cessation Therapy
Detrol LA
Administration route: Oral
Indication: Bladder Disorder
Start date: 2007-01-01
End date: 2007-01-01
Lortab
Indication: Musculoskeletal Pain
Lortab
Indication: Pain in Extremity
Other drugs received by patient: Aggrenox; Prozac; Xanax; Synthroid; Gabapentin; Triamterene; Polyethylene Glycol; Metoclopramide; Metoclopramide; Omeprazole; Omeprazole; Nitroglycerin
Adverse event in female receiving Lortab (Hydrocodone / Acetaminophen)
Reported by a health professional (non-physician/pharmacist) from United States on 2007-05-10
Patient: female, weighing 125.6 kg (276.4 pounds)
Adverse reactions / side effects: Pruritus, Drug Ineffective, Nausea, Pharmaceutical Product Complaint
Suspect drug(s):
Lortab
Dosage: #90 day supply 1 three times/day per oram
Indication: Neuropathy Peripheral
Start date: 1995-01-01
Lortab
Dosage: #90 day supply 1 three times/day per oram
Indication: Pain
Start date: 1995-01-01
Adverse event in female receiving Lortab (Hydrocodone / Acetaminophen)
Reported by a physician from United States on 2007-01-27
Patient: female, weighing 63.6 kg (139.8 pounds)
Adverse reactions / side effects: Hypersensitivity, Pruritus, Anaemia, Rash, Cerebrovascular Accident
Suspect drug(s):
Lortab
Administration route: Oral
Indication: Pain
Start date: 2006-09-06
End date: 2006-09-22
Metaxalone
Administration route: Oral
Indication: Pain
Start date: 2006-09-06
End date: 2006-09-22
Synthroid
Administration route: Oral
Indication: Hypothyroidism
Start date: 2001-10-30
Synthroid
Administration route: Oral
Start date: 1999-01-01
End date: 2001-10-29
Other drugs received by patient: Clonidine; Zestoretic; Celecoxib; Clopidogrel Bisulfate; Zocor; Diphenhydramine Hydrochloride; Lansoprazole; Methocarbamol; Aspirin; Crestor
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