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

HYPOAESTHESIA ( 6 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 4 FDA reports)
HYPOAESTHESIA ORAL ( 4 FDA reports)
STRESS ( 4 FDA reports)
RASH GENERALISED ( 4 FDA reports)
BLOOD CREATINE PHOSPHOKINASE ABNORMAL ( 4 FDA reports)
PRURITUS ( 4 FDA reports)
COMPLETED SUICIDE ( 4 FDA reports)
CONCOMITANT DISEASE PROGRESSION ( 4 FDA reports)
PLATELET COUNT DECREASED ( 4 FDA reports)
INSOMNIA ( 4 FDA reports)
DEAFNESS ( 4 FDA reports)
DEPRESSION ( 4 FDA reports)
CONDITION AGGRAVATED ( 3 FDA reports)
FALL ( 3 FDA reports)
APHASIA ( 2 FDA reports)
DIABETES MELLITUS ( 2 FDA reports)
VOMITING ( 2 FDA reports)
UNRESPONSIVE TO STIMULI ( 2 FDA reports)
DIZZINESS ( 2 FDA reports)
THROMBOTIC MICROANGIOPATHY ( 2 FDA reports)
SKIN DISCOLOURATION ( 2 FDA reports)
BLINDNESS ( 2 FDA reports)
DYSPNOEA ( 2 FDA reports)
PRODUCT QUALITY ISSUE ( 2 FDA reports)
POSTPARTUM HAEMORRHAGE ( 2 FDA reports)
EYE MOVEMENT DISORDER ( 2 FDA reports)
PNEUMONIA ASPIRATION ( 2 FDA reports)
PAIN OF SKIN ( 2 FDA reports)
FEELING ABNORMAL ( 2 FDA reports)
FLUSHING ( 2 FDA reports)
PAIN ( 2 FDA reports)
OXYGEN SATURATION DECREASED ( 2 FDA reports)
OVERDOSE ( 2 FDA reports)
NONSPECIFIC REACTION ( 2 FDA reports)
NAUSEA ( 2 FDA reports)
MYDRIASIS ( 2 FDA reports)
HYPONATRAEMIA ( 1 FDA reports)
CRYOGLOBULINAEMIA ( 1 FDA reports)
JAW DISORDER ( 1 FDA reports)
MUSCLE TWITCHING ( 1 FDA reports)
DEHYDRATION ( 1 FDA reports)
ABDOMINAL PAIN ( 1 FDA reports)
NEPHRITIS AUTOIMMUNE ( 1 FDA reports)
NIGHTMARE ( 1 FDA reports)
HYPERSENSITIVITY ( 1 FDA reports)
HEART RATE INCREASED ( 1 FDA reports)
GASTRIC POLYPS ( 1 FDA reports)
FOOD INTOLERANCE ( 1 FDA reports)
FEAR ( 1 FDA reports)
PANIC ATTACK ( 1 FDA reports)
PARAESTHESIA ( 1 FDA reports)
COUGH ( 1 FDA reports)
DEATH ( 1 FDA reports)
ERYTHEMA MULTIFORME ( 1 FDA reports)
PRODUCT MEASURED POTENCY ISSUE ( 1 FDA reports)
ECZEMA ( 1 FDA reports)
BREATH SOUNDS ABNORMAL ( 1 FDA reports)
PYREXIA ( 1 FDA reports)
RASH ( 1 FDA reports)
DRUG ERUPTION ( 1 FDA reports)
RENAL VESSEL DISORDER ( 1 FDA reports)
SKIN BURNING SENSATION ( 1 FDA reports)
DRUG EFFECT INCREASED ( 1 FDA reports)
ASTHMA ( 1 FDA reports)
THROAT TIGHTNESS ( 1 FDA reports)
DRUG ADMINISTRATION ERROR ( 1 FDA reports)
DISORIENTATION ( 1 FDA reports)
URTICARIA ( 1 FDA reports)
DIFFICULTY IN WALKING ( 1 FDA reports)
ABDOMINAL DISCOMFORT ( 1 FDA reports)

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