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GENERAL PHYSICAL HEALTH DETERIORATION ( 8 FDA reports)
RHEUMATOID ARTHRITIS ( 8 FDA reports)
CONDITION AGGRAVATED ( 7 FDA reports)
ASPERGILLOMA ( 6 FDA reports)
DRUG EFFECT DECREASED ( 6 FDA reports)
INFECTION ( 6 FDA reports)
INFLAMMATION ( 6 FDA reports)
JOINT DESTRUCTION ( 6 FDA reports)
SINUSITIS ASPERGILLUS ( 6 FDA reports)
RENAL FAILURE ACUTE ( 5 FDA reports)
NEPHROTIC SYNDROME ( 4 FDA reports)
RESPIRATORY DISTRESS ( 4 FDA reports)
CARDIAC TAMPONADE ( 3 FDA reports)
DYSPNOEA ( 3 FDA reports)
LIP AND/OR ORAL CAVITY CANCER ( 3 FDA reports)
NO ADVERSE EVENT ( 3 FDA reports)
OLIGURIA ( 3 FDA reports)
RESPIRATORY FAILURE ( 3 FDA reports)
TENDON RUPTURE ( 3 FDA reports)
CONCOMITANT DISEASE AGGRAVATED ( 2 FDA reports)
CUTANEOUS LUPUS ERYTHEMATOSUS ( 2 FDA reports)
DISEASE PROGRESSION ( 2 FDA reports)
DISORIENTATION ( 2 FDA reports)
DRUG DISPENSING ERROR ( 2 FDA reports)
ERYTHEMA ( 2 FDA reports)
FALL ( 2 FDA reports)
FATIGUE ( 2 FDA reports)
HYPOTENSION ( 2 FDA reports)
INFARCTION ( 2 FDA reports)
INTERCEPTED DRUG ADMINISTRATION ERROR ( 2 FDA reports)
MALAISE ( 2 FDA reports)
MYALGIA ( 2 FDA reports)
PAIN IN EXTREMITY ( 2 FDA reports)
PRURITUS ( 2 FDA reports)
VERTIGO ( 2 FDA reports)
ABDOMINAL PAIN ( 1 FDA reports)
AGGRESSION ( 1 FDA reports)
ANAPHYLACTIC SHOCK ( 1 FDA reports)
ANGIOEDEMA ( 1 FDA reports)
ASTHENIA ( 1 FDA reports)
BLADDER PROLAPSE ( 1 FDA reports)
BLOOD CREATININE INCREASED ( 1 FDA reports)
CHEST PAIN ( 1 FDA reports)
CHILLS ( 1 FDA reports)
CHROMATURIA ( 1 FDA reports)
CONFUSIONAL STATE ( 1 FDA reports)
CONTUSION ( 1 FDA reports)
DEEP VEIN THROMBOSIS ( 1 FDA reports)
DELIRIUM ( 1 FDA reports)
DEPRESSION ( 1 FDA reports)
DISCOMFORT ( 1 FDA reports)
DRUG ABUSE ( 1 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 1 FDA reports)
ECCHYMOSIS ( 1 FDA reports)
EPILEPSY ( 1 FDA reports)
ESCHERICHIA URINARY TRACT INFECTION ( 1 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 1 FDA reports)
GRAND MAL CONVULSION ( 1 FDA reports)
HAEMATOMA ( 1 FDA reports)
HAEMATURIA ( 1 FDA reports)
HAEMOLYTIC ANAEMIA ( 1 FDA reports)
HEPATIC ENZYME INCREASED ( 1 FDA reports)
HEPATIC FAILURE ( 1 FDA reports)
HYPERCHOLESTEROLAEMIA ( 1 FDA reports)
HYPERTRIGLYCERIDAEMIA ( 1 FDA reports)
HYPOALBUMINAEMIA ( 1 FDA reports)
HYPOGLYCAEMIA ( 1 FDA reports)
HYPOPROTEINAEMIA ( 1 FDA reports)
INCOHERENT ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 1 FDA reports)
INTERSTITIAL LUNG DISEASE ( 1 FDA reports)
ISCHAEMIC STROKE ( 1 FDA reports)
JAUNDICE ( 1 FDA reports)
JOINT SPRAIN ( 1 FDA reports)
LOSS OF CONSCIOUSNESS ( 1 FDA reports)
MEDICATION ERROR ( 1 FDA reports)
MITRAL VALVE REPLACEMENT ( 1 FDA reports)
MIXED LIVER INJURY ( 1 FDA reports)
MUSCLE RUPTURE ( 1 FDA reports)
MUSCLE SPASMS ( 1 FDA reports)
MUSCULAR WEAKNESS ( 1 FDA reports)
NAUSEA ( 1 FDA reports)
OXYGEN SATURATION ABNORMAL ( 1 FDA reports)
PARAESTHESIA ( 1 FDA reports)
POST PROCEDURAL COMPLICATION ( 1 FDA reports)
PRODUCT QUALITY ISSUE ( 1 FDA reports)
PROTEINURIA ( 1 FDA reports)
RASH MORBILLIFORM ( 1 FDA reports)
RASH PRURITIC ( 1 FDA reports)
RENAL CELL CARCINOMA ( 1 FDA reports)
RENAL FAILURE ( 1 FDA reports)
RENAL NEOPLASM ( 1 FDA reports)
RETINAL HAEMORRHAGE ( 1 FDA reports)
RETINAL VEIN OCCLUSION ( 1 FDA reports)
RETINAL VEIN THROMBOSIS ( 1 FDA reports)
SELF-MEDICATION ( 1 FDA reports)
SKIN GRAFT ( 1 FDA reports)
SKIN NEOPLASM EXCISION ( 1 FDA reports)
SPEECH DISORDER ( 1 FDA reports)
SQUAMOUS CELL CARCINOMA ( 1 FDA reports)
SUBDURAL HAEMATOMA ( 1 FDA reports)
TENDONITIS ( 1 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 1 FDA reports)
THROMBOCYTOPENIC PURPURA ( 1 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 1 FDA reports)
TUBULOINTERSTITIAL NEPHRITIS ( 1 FDA reports)
URTICARIA ( 1 FDA reports)
VOMITING ( 1 FDA reports)

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