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

DIZZINESS ( 10 FDA reports)
SYNCOPE ( 5 FDA reports)
ANAEMIA ( 4 FDA reports)
BLOOD PRESSURE INCREASED ( 4 FDA reports)
CANDIDIASIS ( 3 FDA reports)
DEHYDRATION ( 3 FDA reports)
FEELING ABNORMAL ( 3 FDA reports)
NAUSEA ( 3 FDA reports)
SINUSITIS ( 3 FDA reports)
VOMITING ( 3 FDA reports)
ANKLE FRACTURE ( 2 FDA reports)
ARRHYTHMIA ( 2 FDA reports)
BLISTER ( 2 FDA reports)
BRADYCARDIA ( 2 FDA reports)
CARDIAC PACEMAKER MALFUNCTION ( 2 FDA reports)
CELLULITIS ( 2 FDA reports)
CHEST PAIN ( 2 FDA reports)
CONVULSION ( 2 FDA reports)
DEEP VEIN THROMBOSIS ( 2 FDA reports)
DYSPNOEA ( 2 FDA reports)
FALL ( 2 FDA reports)
FOOT FRACTURE ( 2 FDA reports)
HEADACHE ( 2 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 2 FDA reports)
LIGAMENT INJURY ( 2 FDA reports)
LOSS OF CONSCIOUSNESS ( 2 FDA reports)
MULTIPLE SCLEROSIS RELAPSE ( 2 FDA reports)
OEDEMA PERIPHERAL ( 2 FDA reports)
PAIN ( 2 FDA reports)
PANCYTOPENIA ( 2 FDA reports)
PRURITUS ( 2 FDA reports)
STEVENS-JOHNSON SYNDROME ( 2 FDA reports)
VERTIGO ( 2 FDA reports)
ABDOMINAL PAIN UPPER ( 1 FDA reports)
AGGRESSION ( 1 FDA reports)
ALOPECIA ( 1 FDA reports)
ANGER ( 1 FDA reports)
ANGIONEUROTIC OEDEMA ( 1 FDA reports)
ARTHRALGIA ( 1 FDA reports)
ASTHENIA ( 1 FDA reports)
ATELECTASIS ( 1 FDA reports)
BACK PAIN ( 1 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 1 FDA reports)
BLOOD BICARBONATE DECREASED ( 1 FDA reports)
BODY TEMPERATURE INCREASED ( 1 FDA reports)
BRAIN STEM INFARCTION ( 1 FDA reports)
BRONCHITIS ( 1 FDA reports)
CARDIOVASCULAR FUNCTION TEST ABNORMAL ( 1 FDA reports)
CAROTID ARTERY STENOSIS ( 1 FDA reports)
CEREBROVASCULAR ACCIDENT ( 1 FDA reports)
CHEILITIS ( 1 FDA reports)
CHILLS ( 1 FDA reports)
CONFUSIONAL STATE ( 1 FDA reports)
CONJUNCTIVAL OEDEMA ( 1 FDA reports)
CONTUSION ( 1 FDA reports)
COORDINATION ABNORMAL ( 1 FDA reports)
DEPRESSION ( 1 FDA reports)
DIPLOPIA ( 1 FDA reports)
DISEASE PROGRESSION ( 1 FDA reports)
DISEASE RECURRENCE ( 1 FDA reports)
DRUG HYPERSENSITIVITY ( 1 FDA reports)
DRUG INEFFECTIVE ( 1 FDA reports)
DRY MOUTH ( 1 FDA reports)
DYSTONIA ( 1 FDA reports)
EPISTAXIS ( 1 FDA reports)
EYE SWELLING ( 1 FDA reports)
FATIGUE ( 1 FDA reports)
FEELING JITTERY ( 1 FDA reports)
FRACTURED COCCYX ( 1 FDA reports)
GASTRIC ULCER ( 1 FDA reports)
HAEMATOCRIT DECREASED ( 1 FDA reports)
HAEMOGLOBIN DECREASED ( 1 FDA reports)
HAEMORRHAGE ( 1 FDA reports)
HALLUCINATION, AUDITORY ( 1 FDA reports)
HEART RATE INCREASED ( 1 FDA reports)
HYPERCHOLESTEROLAEMIA ( 1 FDA reports)
HYPERHIDROSIS ( 1 FDA reports)
HYPERSENSITIVITY ( 1 FDA reports)
IMPAIRED HEALING ( 1 FDA reports)
INFECTION IN AN IMMUNOCOMPROMISED HOST ( 1 FDA reports)
INFLUENZA LIKE ILLNESS ( 1 FDA reports)
INJECTION SITE ERYTHEMA ( 1 FDA reports)
INJECTION SITE NODULE ( 1 FDA reports)
INJECTION SITE PAIN ( 1 FDA reports)
INJECTION SITE REACTION ( 1 FDA reports)
INJECTION SITE SCAR ( 1 FDA reports)
INJECTION SITE SWELLING ( 1 FDA reports)
INJECTION SITE ULCER ( 1 FDA reports)
INJECTION SITE WARMTH ( 1 FDA reports)
INSOMNIA ( 1 FDA reports)
INTERVERTEBRAL DISC DEGENERATION ( 1 FDA reports)
IRON DEFICIENCY ( 1 FDA reports)
JAUNDICE ( 1 FDA reports)
LEFT ATRIAL DILATATION ( 1 FDA reports)
MITRAL VALVE INCOMPETENCE ( 1 FDA reports)
MULTIPLE SCLEROSIS ( 1 FDA reports)
MUSCLE SPASMS ( 1 FDA reports)
MYALGIA ( 1 FDA reports)
NASOPHARYNGITIS ( 1 FDA reports)
NERVOUSNESS ( 1 FDA reports)
NEUROPATHY ( 1 FDA reports)
NEUROPATHY PERIPHERAL ( 1 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING BRAIN ABNORMAL ( 1 FDA reports)
ORAL FUNGAL INFECTION ( 1 FDA reports)
ORTHOSTATIC HYPOTENSION ( 1 FDA reports)
OSTEOARTHRITIS ( 1 FDA reports)
OSTEOPOROSIS ( 1 FDA reports)
PELVIC FRACTURE ( 1 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 1 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 1 FDA reports)
PLEURAL EFFUSION ( 1 FDA reports)
PNEUMONIA ( 1 FDA reports)
POST PROCEDURAL PAIN ( 1 FDA reports)
PRE-EXISTING CONDITION IMPROVED ( 1 FDA reports)
PSYCHOMOTOR HYPERACTIVITY ( 1 FDA reports)
PULMONARY HYPERTENSION ( 1 FDA reports)
PURPURA ( 1 FDA reports)
PYREXIA ( 1 FDA reports)
RASH ( 1 FDA reports)
RASH GENERALISED ( 1 FDA reports)
RENAL COLIC ( 1 FDA reports)
RIB FRACTURE ( 1 FDA reports)
SUICIDAL BEHAVIOUR ( 1 FDA reports)
SWELLING ( 1 FDA reports)
SWELLING FACE ( 1 FDA reports)
TREATMENT NONCOMPLIANCE ( 1 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 1 FDA reports)
TRIGEMINAL NEURALGIA ( 1 FDA reports)
UNEVALUABLE EVENT ( 1 FDA reports)
URINARY INCONTINENCE ( 1 FDA reports)
URTICARIA ( 1 FDA reports)

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