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

DIARRHOEA ( 24 FDA reports)
VOMITING ( 20 FDA reports)
TOOTH DISCOLOURATION ( 14 FDA reports)
DRUG INEFFECTIVE ( 9 FDA reports)
PYREXIA ( 9 FDA reports)
URTICARIA ( 9 FDA reports)
MEDICATION ERROR ( 7 FDA reports)
RASH ( 7 FDA reports)
DERMATITIS ACNEIFORM ( 6 FDA reports)
ECZEMA ( 6 FDA reports)
MALIGNANT MELANOMA STAGE I ( 6 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 6 FDA reports)
BRONCHITIS ( 5 FDA reports)
CHILLS ( 5 FDA reports)
DYSPLASTIC NAEVUS SYNDROME ( 5 FDA reports)
MELANOCYTIC NAEVUS ( 5 FDA reports)
OVERDOSE ( 5 FDA reports)
PRURITUS ( 5 FDA reports)
SKIN NEOPLASM EXCISION ( 5 FDA reports)
ASTHMA ( 4 FDA reports)
DERMATITIS BULLOUS ( 4 FDA reports)
DERMATITIS DIAPER ( 4 FDA reports)
DYSPNOEA ( 4 FDA reports)
OROPHARYNGEAL PAIN ( 4 FDA reports)
PRODUCTIVE COUGH ( 4 FDA reports)
PURULENT DISCHARGE ( 4 FDA reports)
RASH MACULAR ( 4 FDA reports)
RETCHING ( 4 FDA reports)
WOUND INFECTION ( 4 FDA reports)
ANGIONEUROTIC OEDEMA ( 3 FDA reports)
DYSGEUSIA ( 3 FDA reports)
MUSCLE CRAMP ( 3 FDA reports)
OEDEMA PERIPHERAL ( 3 FDA reports)
PAIN IN EXTREMITY ( 3 FDA reports)
RASH GENERALISED ( 3 FDA reports)
SWELLING ( 3 FDA reports)
ABDOMINAL PAIN UPPER ( 2 FDA reports)
ABNORMAL BEHAVIOUR ( 2 FDA reports)
ACCIDENTAL OVERDOSE ( 2 FDA reports)
AGGRESSION ( 2 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 2 FDA reports)
ANXIETY ( 2 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 2 FDA reports)
CHOLESTASIS ( 2 FDA reports)
DERMATITIS ALLERGIC ( 2 FDA reports)
DIZZINESS ( 2 FDA reports)
DYSPHAGIA ( 2 FDA reports)
ERYTHEMA MULTIFORME ( 2 FDA reports)
FUNGAL INFECTION ( 2 FDA reports)
HEPATOTOXICITY ( 2 FDA reports)
INFLAMMATION ( 2 FDA reports)
IRRITABILITY ( 2 FDA reports)
JAUNDICE ( 2 FDA reports)
LIVER TRANSPLANT ( 2 FDA reports)
NAUSEA ( 2 FDA reports)
PAIN ( 2 FDA reports)
PSYCHOMOTOR HYPERACTIVITY ( 2 FDA reports)
RASH ERYTHEMATOUS ( 2 FDA reports)
RASH PRURITIC ( 2 FDA reports)
SCAR ( 2 FDA reports)
SCLERAL DISCOLOURATION ( 2 FDA reports)
STEVENS-JOHNSON SYNDROME ( 2 FDA reports)
SUTURE RELATED COMPLICATION ( 2 FDA reports)
ABDOMINAL PAIN ( 1 FDA reports)
ANGER ( 1 FDA reports)
ANOREXIA ( 1 FDA reports)
AUTISM ( 1 FDA reports)
BILE DUCT OBSTRUCTION ( 1 FDA reports)
BIOPSY LIVER ( 1 FDA reports)
BLISTER ( 1 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 1 FDA reports)
BLOOD BILIRUBIN INCREASED ( 1 FDA reports)
BLOOD CALCIUM INCREASED ( 1 FDA reports)
BLOOD CREATININE INCREASED ( 1 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 1 FDA reports)
BLOOD UREA INCREASED ( 1 FDA reports)
CHALAZION ( 1 FDA reports)
CHROMATURIA ( 1 FDA reports)
CLOSTRIDIUM COLITIS ( 1 FDA reports)
CONFUSIONAL STATE ( 1 FDA reports)
CRYING ( 1 FDA reports)
CYTOLYTIC HEPATITIS ( 1 FDA reports)
DEHYDRATION ( 1 FDA reports)
DEPRESSION ( 1 FDA reports)
DIABETES MELLITUS ( 1 FDA reports)
DIPLOPIA ( 1 FDA reports)
DISORIENTATION ( 1 FDA reports)
DRUG DISPENSING ERROR ( 1 FDA reports)
DRUG HYPERSENSITIVITY ( 1 FDA reports)
DRUG INTOLERANCE ( 1 FDA reports)
DRUG PRESCRIBING ERROR ( 1 FDA reports)
DYSKINESIA ( 1 FDA reports)
DYSPEPSIA ( 1 FDA reports)
EAR INFECTION ( 1 FDA reports)
ECZEMA NUMMULAR ( 1 FDA reports)
ERYSIPELAS ( 1 FDA reports)
ERYTHEMA ( 1 FDA reports)
FACE OEDEMA ( 1 FDA reports)
FAECES DISCOLOURED ( 1 FDA reports)
FEELING ABNORMAL ( 1 FDA reports)
GASTROINTESTINAL DISORDER ( 1 FDA reports)
HALLUCINATION ( 1 FDA reports)
HEADACHE ( 1 FDA reports)
HEPATIC NECROSIS ( 1 FDA reports)
HEPATITIS ( 1 FDA reports)
HEPATITIS VIRAL ( 1 FDA reports)
HYPERSENSITIVITY ( 1 FDA reports)
INSOMNIA ( 1 FDA reports)
LINEAR IGA DISEASE ( 1 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 1 FDA reports)
LIVER INJURY ( 1 FDA reports)
LOOSE STOOLS ( 1 FDA reports)
LUNG DISORDER ( 1 FDA reports)
MANIA ( 1 FDA reports)
MASTICATION DISORDER ( 1 FDA reports)
MIXED LIVER INJURY ( 1 FDA reports)
MOOD ALTERED ( 1 FDA reports)
MYALGIA ( 1 FDA reports)
OESOPHAGEAL PAIN ( 1 FDA reports)
ORAL DISCOMFORT ( 1 FDA reports)
OTITIS MEDIA ACUTE ( 1 FDA reports)
PALMAR-PLANTAR ERYTHRODYSAESTHESIA SYNDROME ( 1 FDA reports)
PRESCRIBED OVERDOSE ( 1 FDA reports)
PRODUCT QUALITY ISSUE ( 1 FDA reports)
PROTEIN URINE PRESENT ( 1 FDA reports)
PRURIGO ( 1 FDA reports)
RASH MACULO-PAPULAR ( 1 FDA reports)
RASH PAPULAR ( 1 FDA reports)
SCREAMING ( 1 FDA reports)
SECRETION DISCHARGE ( 1 FDA reports)
SERUM SICKNESS ( 1 FDA reports)
SKIN LESION ( 1 FDA reports)
SLEEP DISORDER ( 1 FDA reports)
SLEEP TALKING ( 1 FDA reports)
SOMNOLENCE ( 1 FDA reports)
SPEECH DISORDER ( 1 FDA reports)
STRABISMUS ( 1 FDA reports)
TONGUE BITING ( 1 FDA reports)
TONGUE DESQUAMATION ( 1 FDA reports)
TONGUE DISCOLOURATION ( 1 FDA reports)
TONGUE HAEMORRHAGE ( 1 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 1 FDA reports)
TOXIC SKIN ERUPTION ( 1 FDA reports)
TYMPANIC MEMBRANE PERFORATION ( 1 FDA reports)
VOMITING PROJECTILE ( 1 FDA reports)
WEIGHT DECREASED ( 1 FDA reports)
WEIGHT INCREASED ( 1 FDA reports)

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