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Index of reports
> All cases (2)
Below is the selection of adverse event reports related to Levothroid (Levothyroxine) that includes all cases.
Adverse event in 39 year old female receiving Levothroid (Levothyroxine)
Reported by a consumer/non-health professional from United States on 2007-07-25
Patient: 39 year old female
Adverse reactions / side effects: Blood Thyroid Stimulating Hormone Decreased, Hepatic Steatosis
Suspect drug(s):
Levothroid
Dosage: 112 mcg qd; po
Administration route: Oral
Indication: Hypothyroidism
Start date: 2005-01-01
End date: 2007-07-01
Levothroid
Dosage: 110 mcg qd; po
Administration route: Oral
Indication: Hypothyroidism
End date: 2005-01-01
Levothroid
Dosage: 125 mcg qd;po
Administration route: Oral
Indication: Hypothyroidism
Start date: 2007-07-02
Adverse event in 68 year old female receiving Levothroid (Levothyroxine)
Reported by a individual with unspecified qualification from United States on 2007-01-29
Patient: 68 year old female, weighing 81.6 kg (179.6 pounds)
Adverse reactions / side effects: Weight Increased, Fatigue, Alopecia, DRY Skin, Gastrooesophageal Reflux Disease
Suspect drug(s):
Levothroid
Dosage: 125 mcg qd po
Administration route: Oral
Indication: Hypothyroidism
Start date: 2006-05-01
End date: 2006-07-01
Levothroid
Dosage: 125 mcg qd po
Administration route: Oral
Indication: Hypothyroidism
Start date: 2006-08-01
Levothroid
Dosage: 125 mcg q07od po
Administration route: Oral
Indication: Hypothyroidism
Start date: 2006-07-01
End date: 2006-08-01
Levothroid
Dosage: 62.5 mg qod po
Administration route: Oral
Indication: Hypothyroidism
Start date: 2006-07-01
End date: 2006-08-01
Levothroid
Dosage: 150 mcg qd po
Administration route: Oral
Indication: Hypothyroidism
Start date: 2004-01-01
End date: 2006-05-01
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