Please choose an event type to view the corresponding MedsFacts report:

COUGH ( 5 FDA reports)
DRUG INEFFECTIVE ( 4 FDA reports)
DRY THROAT ( 4 FDA reports)
FATIGUE ( 4 FDA reports)
DYSPHONIA ( 4 FDA reports)
FALL ( 4 FDA reports)
PAROSMIA ( 3 FDA reports)
AGEUSIA ( 3 FDA reports)
ANOSMIA ( 3 FDA reports)
PALLOR ( 3 FDA reports)
ORAL CANDIDIASIS ( 3 FDA reports)
DEHYDRATION ( 3 FDA reports)
HYPOKINESIA ( 3 FDA reports)
HYPERHIDROSIS ( 3 FDA reports)
TREMOR ( 2 FDA reports)
PANIC REACTION ( 2 FDA reports)
AORTICOPULMONARY SEPTAL DEFECT ( 2 FDA reports)
ATRIAL SEPTAL DEFECT ( 2 FDA reports)
OROPHARYNGEAL PAIN ( 2 FDA reports)
ODYNOPHAGIA ( 2 FDA reports)
NAUSEA ( 2 FDA reports)
MYOCLONUS ( 2 FDA reports)
MALAISE ( 2 FDA reports)
LYMPH NODE PAIN ( 2 FDA reports)
INTERRUPTION OF AORTIC ARCH ( 2 FDA reports)
DEPENDENCE ( 2 FDA reports)
INSOMNIA ( 2 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 2 FDA reports)
DYSPNOEA ( 2 FDA reports)
ENZYME ABNORMALITY ( 1 FDA reports)
FAECES DISCOLOURED ( 1 FDA reports)
DYSSTASIA ( 1 FDA reports)
DYSPEPSIA ( 1 FDA reports)
FLATULENCE ( 1 FDA reports)
HEPATIC ENZYME INCREASED ( 1 FDA reports)
HIP FRACTURE ( 1 FDA reports)
DRUG EFFECT INCREASED ( 1 FDA reports)
DIZZINESS ( 1 FDA reports)
ILL-DEFINED DISORDER ( 1 FDA reports)
INCONTINENCE ( 1 FDA reports)
INFECTION ( 1 FDA reports)
DIARRHOEA ( 1 FDA reports)
DECREASED APPETITE ( 1 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 1 FDA reports)
CIRCULATORY COLLAPSE ( 1 FDA reports)
CHEST PAIN ( 1 FDA reports)
MONOPLEGIA ( 1 FDA reports)
MUSCLE SPASMS ( 1 FDA reports)
BRONCHITIS ( 1 FDA reports)
NASAL ULCER ( 1 FDA reports)
NASOPHARYNGITIS ( 1 FDA reports)
BLUNTED AFFECT ( 1 FDA reports)
NIGHTMARE ( 1 FDA reports)
BLOOD PRESSURE INCREASED ( 1 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 1 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 1 FDA reports)
APHONIA ( 1 FDA reports)
PANIC ATTACK ( 1 FDA reports)
AGITATION ( 1 FDA reports)
ABDOMINAL PAIN UPPER ( 1 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 1 FDA reports)
PNEUMONIA ( 1 FDA reports)
PRODUCT QUALITY ISSUE ( 1 FDA reports)
RETCHING ( 1 FDA reports)
SINUS OPERATION ( 1 FDA reports)
SLEEP ATTACKS ( 1 FDA reports)
SLEEP WALKING ( 1 FDA reports)
SOMNOLENCE ( 1 FDA reports)
STOMACH DISCOMFORT ( 1 FDA reports)
SUDDEN ONSET OF SLEEP ( 1 FDA reports)
SUICIDAL IDEATION ( 1 FDA reports)
THROAT IRRITATION ( 1 FDA reports)
ABDOMINAL DISTENSION ( 1 FDA reports)
UPPER LIMB FRACTURE ( 1 FDA reports)
VOMITING ( 1 FDA reports)
WEIGHT INCREASED ( 1 FDA reports)

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