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MUSCLE CONTRACTIONS INVOLUNTARY ( 17 FDA reports)
EATING DISORDER ( 16 FDA reports)
FALL ( 15 FDA reports)
HALLUCINATION ( 14 FDA reports)
AKATHISIA ( 13 FDA reports)
RASH ERYTHEMATOUS ( 6 FDA reports)
HISTIOCYTOSIS HAEMATOPHAGIC ( 5 FDA reports)
ARTHRITIS ( 5 FDA reports)
NAUSEA ( 4 FDA reports)
PANCREATITIS ( 3 FDA reports)
HYPERSENSITIVITY ( 3 FDA reports)
ATELECTASIS ( 3 FDA reports)
CONDITION AGGRAVATED ( 3 FDA reports)
VOMITING ( 2 FDA reports)
BLOOD PRESSURE DECREASED ( 2 FDA reports)
RESPIRATORY DISORDER ( 2 FDA reports)
INFLAMMATION ( 2 FDA reports)
PYREXIA ( 2 FDA reports)
PRURITUS ( 2 FDA reports)
PAIN ( 2 FDA reports)
OEDEMA PERIPHERAL ( 2 FDA reports)
NIGHT SWEATS ( 2 FDA reports)
AGGRESSION ( 2 FDA reports)
MENTAL DISORDER ( 2 FDA reports)
LOCALISED INFECTION ( 2 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 2 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 2 FDA reports)
ANGER ( 2 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 2 FDA reports)
FLUSHING ( 2 FDA reports)
APPLICATION SITE REACTION ( 2 FDA reports)
FATIGUE ( 1 FDA reports)
EYE ROLLING ( 1 FDA reports)
HAEMOGLOBIN DECREASED ( 1 FDA reports)
DYSPNOEA ( 1 FDA reports)
HEPATITIS ( 1 FDA reports)
ANAPHYLACTIC REACTION ( 1 FDA reports)
DYSKINESIA ( 1 FDA reports)
HYPOPHAGIA ( 1 FDA reports)
HYPOTENSION ( 1 FDA reports)
BLOOD POTASSIUM INCREASED ( 1 FDA reports)
INFUSION SITE REACTION ( 1 FDA reports)
INJECTION SITE PRURITUS ( 1 FDA reports)
INJECTION SITE REACTION ( 1 FDA reports)
INJECTION SITE WARMTH ( 1 FDA reports)
INSOMNIA ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 1 FDA reports)
JAUNDICE ( 1 FDA reports)
JUVENILE ARTHRITIS ( 1 FDA reports)
DRUG INEFFECTIVE ( 1 FDA reports)
LOSS OF CONSCIOUSNESS ( 1 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 1 FDA reports)
MALAISE ( 1 FDA reports)
DISEASE PROGRESSION ( 1 FDA reports)
DERMATITIS ( 1 FDA reports)
ABNORMAL DREAMS ( 1 FDA reports)
DEHYDRATION ( 1 FDA reports)
CONVULSION ( 1 FDA reports)
OFF LABEL USE ( 1 FDA reports)
ONYCHOCLASIS ( 1 FDA reports)
ORAL PRURITUS ( 1 FDA reports)
BLISTER ( 1 FDA reports)
PAIN IN EXTREMITY ( 1 FDA reports)
ABDOMINAL PAIN UPPER ( 1 FDA reports)
PARTIAL SEIZURES ( 1 FDA reports)
PROTEINURIA ( 1 FDA reports)
CARDIO-RESPIRATORY ARREST ( 1 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 1 FDA reports)
RASH ( 1 FDA reports)
BRAIN OEDEMA ( 1 FDA reports)
RENAL FAILURE ACUTE ( 1 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 1 FDA reports)
SJOGREN'S SYNDROME ( 1 FDA reports)
SKIN FISSURES ( 1 FDA reports)
SKIN PLAQUE ( 1 FDA reports)
SLEEP DISORDER ( 1 FDA reports)
SYNCOPE ( 1 FDA reports)
THROAT TIGHTNESS ( 1 FDA reports)
THROMBOCYTOPENIA ( 1 FDA reports)
VISION BLURRED ( 1 FDA reports)
ABDOMINAL DISTENSION ( 1 FDA reports)

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