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

RASH ( 8 FDA reports)
OEDEMA PERIPHERAL ( 5 FDA reports)
PAIN ( 5 FDA reports)
DIARRHOEA ( 4 FDA reports)
ERYTHEMA ( 4 FDA reports)
PRURITUS ( 4 FDA reports)
URTICARIA ( 4 FDA reports)
ASTHENIA ( 3 FDA reports)
BLOOD PRESSURE INCREASED ( 3 FDA reports)
BURNING SENSATION ( 3 FDA reports)
DERMATITIS ( 3 FDA reports)
DYSPHAGIA ( 3 FDA reports)
DYSPNOEA ( 3 FDA reports)
EMOTIONAL DISTRESS ( 3 FDA reports)
HEART RATE INCREASED ( 3 FDA reports)
HYPERSENSITIVITY ( 3 FDA reports)
HYPOGLYCAEMIA ( 3 FDA reports)
LYMPHADENOPATHY ( 3 FDA reports)
MALNUTRITION ( 3 FDA reports)
PHARYNGEAL OEDEMA ( 3 FDA reports)
POOR QUALITY SLEEP ( 3 FDA reports)
SKIN ULCER ( 3 FDA reports)
SWOLLEN TONGUE ( 3 FDA reports)
URINARY TRACT INFECTION ( 3 FDA reports)
ACCIDENTAL OVERDOSE ( 2 FDA reports)
ALOPECIA ( 2 FDA reports)
AMNESIA ( 2 FDA reports)
APPLICATION SITE DISCOLOURATION ( 2 FDA reports)
ATROPHY ( 2 FDA reports)
BALANCE DISORDER ( 2 FDA reports)
BLINDNESS ( 2 FDA reports)
BLOOD DISORDER ( 2 FDA reports)
CARDIAC DISORDER ( 2 FDA reports)
CARDIAC FAILURE ( 2 FDA reports)
CATARACT ( 2 FDA reports)
CHEMICAL POISONING ( 2 FDA reports)
CHOKING ( 2 FDA reports)
COUGH ( 2 FDA reports)
DEPRESSION ( 2 FDA reports)
DIZZINESS ( 2 FDA reports)
EATING DISORDER ( 2 FDA reports)
ERYTHEMA MULTIFORME ( 2 FDA reports)
EYE DISORDER ( 2 FDA reports)
EYE INFLAMMATION ( 2 FDA reports)
HEADACHE ( 2 FDA reports)
HEART INJURY ( 2 FDA reports)
HEPATITIS ( 2 FDA reports)
HYPERCHLORHYDRIA ( 2 FDA reports)
HYPERKALAEMIA ( 2 FDA reports)
HYPERTENSION ( 2 FDA reports)
HYPOACUSIS ( 2 FDA reports)
HYPOKALAEMIA ( 2 FDA reports)
ILL-DEFINED DISORDER ( 2 FDA reports)
ILLUSION ( 2 FDA reports)
INSOMNIA ( 2 FDA reports)
JAUNDICE ( 2 FDA reports)
LETHARGY ( 2 FDA reports)
LIP SWELLING ( 2 FDA reports)
MEDICATION ERROR ( 2 FDA reports)
MUSCLE ATROPHY ( 2 FDA reports)
MUSCLE SPASMS ( 2 FDA reports)
ORAL PAIN ( 2 FDA reports)
PNEUMONITIS ( 2 FDA reports)
STEVENS-JOHNSON SYNDROME ( 2 FDA reports)
SWELLING ( 2 FDA reports)
SYNCOPE ( 2 FDA reports)
TEMPERATURE REGULATION DISORDER ( 2 FDA reports)
THROAT IRRITATION ( 2 FDA reports)
TINNITUS ( 2 FDA reports)
VARICELLA ( 2 FDA reports)
VISION BLURRED ( 2 FDA reports)
VISUAL ACUITY REDUCED ( 2 FDA reports)
WEIGHT DECREASED ( 2 FDA reports)
WRIST FRACTURE ( 2 FDA reports)
ACCIDENT ( 1 FDA reports)
ADVERSE EVENT ( 1 FDA reports)
ANAPHYLACTIC REACTION ( 1 FDA reports)
ANGIOEDEMA ( 1 FDA reports)
BLOOD GLUCOSE INCREASED ( 1 FDA reports)
CHROMATURIA ( 1 FDA reports)
DECREASED APPETITE ( 1 FDA reports)
DERMATITIS BULLOUS ( 1 FDA reports)
DRUG TOXICITY ( 1 FDA reports)
DYSPNOEA EXERTIONAL ( 1 FDA reports)
EAR INFECTION ( 1 FDA reports)
EYE HAEMORRHAGE ( 1 FDA reports)
EYE INJURY ( 1 FDA reports)
EYELID OEDEMA ( 1 FDA reports)
FATIGUE ( 1 FDA reports)
FEELING HOT ( 1 FDA reports)
HEARING IMPAIRED ( 1 FDA reports)
HEPATIC NEOPLASM MALIGNANT ( 1 FDA reports)
INFLAMMATION ( 1 FDA reports)
LUNG DISORDER ( 1 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 1 FDA reports)
MULTI-ORGAN DISORDER ( 1 FDA reports)
MYALGIA ( 1 FDA reports)
OCULAR HYPERAEMIA ( 1 FDA reports)
OEDEMA ( 1 FDA reports)
OXYGEN SATURATION DECREASED ( 1 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 1 FDA reports)
PYREXIA ( 1 FDA reports)
RASH ERYTHEMATOUS ( 1 FDA reports)
RASH MACULO-PAPULAR ( 1 FDA reports)
RASH PRURITIC ( 1 FDA reports)
RASH PUSTULAR ( 1 FDA reports)
SKIN SWELLING ( 1 FDA reports)
SKIN WARM ( 1 FDA reports)
SYSTEMIC CANDIDA ( 1 FDA reports)
TACHYCARDIA ( 1 FDA reports)
TOOTH EROSION ( 1 FDA reports)
VISUAL DISTURBANCE ( 1 FDA reports)
VOMITING ( 1 FDA reports)
WHEEZING ( 1 FDA reports)

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