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

BURSITIS ( 7 FDA reports)
CARDIAC FAILURE ( 5 FDA reports)
CELLULITIS ( 4 FDA reports)
PYREXIA ( 3 FDA reports)
POOR QUALITY DRUG ADMINISTERED ( 3 FDA reports)
PERIPHERAL ISCHAEMIA ( 3 FDA reports)
LOBAR PNEUMONIA ( 3 FDA reports)
INJECTION SITE PAIN ( 3 FDA reports)
INJECTION SITE INFLAMMATION ( 3 FDA reports)
HYPERSENSITIVITY ( 3 FDA reports)
DRUG TOXICITY ( 3 FDA reports)
DIABETES MELLITUS ( 3 FDA reports)
INJECTION SITE OEDEMA ( 2 FDA reports)
CONDITION AGGRAVATED ( 2 FDA reports)
DISEASE PROGRESSION ( 2 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 2 FDA reports)
PULMONARY OEDEMA ( 2 FDA reports)
DYSPNOEA ( 2 FDA reports)
PRODUCT COUNTERFEIT ( 2 FDA reports)
PNEUMONIA ( 2 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 2 FDA reports)
PAIN ( 2 FDA reports)
NEUROLEPTIC MALIGNANT SYNDROME ( 2 FDA reports)
HEADACHE ( 2 FDA reports)
ASTHENIA ( 2 FDA reports)
LEG AMPUTATION ( 2 FDA reports)
INCORRECT ROUTE OF DRUG ADMINISTRATION ( 1 FDA reports)
BLOOD PRESSURE INCREASED ( 1 FDA reports)
DECUBITUS ULCER ( 1 FDA reports)
BLOOD ALBUMIN DECREASED ( 1 FDA reports)
INJECTION SITE SWELLING ( 1 FDA reports)
ISCHAEMIA ( 1 FDA reports)
JOINT EFFUSION ( 1 FDA reports)
HYPERTONIA ( 1 FDA reports)
LIP OEDEMA ( 1 FDA reports)
CATATONIA ( 1 FDA reports)
NECROSIS ( 1 FDA reports)
GASTROINTESTINAL PAIN ( 1 FDA reports)
OVERDOSE ( 1 FDA reports)
FEBRILE CONVULSION ( 1 FDA reports)
EYE OEDEMA ( 1 FDA reports)
EYE DISORDER ( 1 FDA reports)
ARTERIOSCLEROSIS OBLITERANS ( 1 FDA reports)
PROCTALGIA ( 1 FDA reports)
ERYTHEMA MULTIFORME ( 1 FDA reports)
CHOREOATHETOSIS ( 1 FDA reports)
DRUG INEFFECTIVE ( 1 FDA reports)
RASH ( 1 FDA reports)
RESPIRATORY DISORDER ( 1 FDA reports)
SALIVARY HYPERSECRETION ( 1 FDA reports)
SKIN NECROSIS ( 1 FDA reports)
STEATORRHOEA ( 1 FDA reports)
TACHYCARDIA ( 1 FDA reports)
VISUAL IMPAIRMENT ( 1 FDA reports)
VITAL FUNCTIONS ABNORMAL ( 1 FDA reports)
VOMITING ( 1 FDA reports)

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